Data / Medical devices / United States / Maquet Cardiovascular LLC
Maquet Cardiovascular LLC: FDA-registered device maker in Wayne, NJ, United States, 12 510(k) clearances
Maquet Cardiovascular LLC is registered with the FDA (registration 2242352) in Wayne, NJ, United States. It lists 10 device types. The FDA files 12 510(k) clearances under its listings, the newest dated April 27, 2026. 40 recall events name it as the recalling firm (3 Class I). Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2242352
- Address
- 45 Barbour Pond Drive, Wayne, NJ, United States, 07470
- Owner or operator
- Maquet Cardiovascular LLC (10024202)
- Roles
- Manufacturer, Specification developer
- First device listed
- January 10, 2008
- Registered through
- 2026
- Brand names listed
- 5MM ENDOSCOPE, 7MM ENDOSCOPE, 7mm Extended Length Endoscope, ACCESSRAIL Platform (Deep Blade), ACCESSRAIL Platform (Standard Blade), ACROBAT-i Vaccum Positioner System, AXIUS XPOSE DEVICE, Acrobat SUV Vacuum Off-Pump System and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Irrigation | GBX | 1 | Manufacturer | accessdata.fda.gov |
| Clamp, Vascular | DXC | 2 | Manufacturer | accessdata.fda.gov |
| Cutter, Surgical | FZT | 1 | Manufacturer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Instruments, Surgical, Cardiovascular | DWS | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Lavage, Jet | FQH | 2 | Manufacturer | accessdata.fda.gov |
| Prosthesis, Vascular Graft, Of 6mm And Greater Diameter | DSY | 2 | Manufacturer | accessdata.fda.gov |
| Prosthesis, Vascular Graft, Of Less Then 6mm Diameter | DYF | 2 | Manufacturer | accessdata.fda.gov |
| Stabilizer, Heart | MWS | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 27, 2026 | K252445 | Fusion Bioline Vascular Graft | DSY | Substantially Equivalent | Maquet Cardiovascular, LLC | accessdata.fda.gov |
| May 30, 2025 | K251238 | Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000); Vasoview Hemopro 3 Endoscopic Vessel Harvesting System with Vasoshield (VH-6001); Vasoview Hemopro 3 Power Supply (VH-6010) | GEI | Substantially Equivalent | Maquet Cardiovascular, LLC | accessdata.fda.gov |
| April 15, 2020 | K191930 | 7 mm Extended Length Endoscope | GCJ | Substantially Equivalent | Maquet Cardiovascular, LLC | accessdata.fda.gov |
| September 17, 2019 | K191947 | VASOVIEW HEMOPRO Extension Cable, VASOVIEW HEMOPRO 2 Extension Cable, Bipolar Extension Cable, Fixed Distance, Active Return Cord | GEI | Substantially Equivalent | Maquet Cardiovascular, LLC | accessdata.fda.gov |
| June 5, 2013 | K130382 | HEARTSTRING III PROXIMAL SEAL SYSTEM | DXC | Substantially Equivalent | Boston Scientific Corporation | accessdata.fda.gov |
| April 11, 2013 | K130121 | SHORT PORT BLUNT TIP TROCAR | GCJ | Substantially Equivalent | Boston Scientific Corporation | accessdata.fda.gov |
| June 11, 2010 | K101274 | VASOVIEW HEMOPRO 2 ENDOSCOPIC VESSEL HARVESTING SYSTEM | GEI | Substantially Equivalent | Maquet Cardiovascular, LLC | accessdata.fda.gov |
| August 28, 2009 | K091733 | VASOVIEW 6 PRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-2500 | GEI | Substantially Equivalent | Maquet Cardiovascular, LLC | accessdata.fda.gov |
| December 17, 2008 | K082725 | GRAFTGUARD PRESSURE CONTROLLING SYRINGE | GBX | Substantially Equivalent | Maquet Cardiovascular, LLC | accessdata.fda.gov |
| August 20, 2004 | K041981 | GUIDANT VASOVIEW 6 HARVESTING CANNULA, MODEL VH-2000; GUIDANT VASOVIEW 6 ACCESSORY PACK, MODEL VH-2004 | GEI | Substantially Equivalent | Guidant Corporation | accessdata.fda.gov |
| April 4, 2001 | K010117 | GUIDANT AXIUS CORONARY SHUNT | DXC | Substantially Equivalent | Cardiothoracic Systems, Inc. | accessdata.fda.gov |
| July 30, 1999 | K992353 | BLUNT TIP TROCAR PORT | GCJ | Substantially Equivalent | Origin Medsystems, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| June 2, 2026 | 99259 | Class II | Ongoing | The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274. | Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run ID 1183-28782A) performed by STERIS at its Whippany, NJ facility between March 31 and April 1 of 2026. | accessdata.fda.gov |
| August 15, 2025 | 97450 | Class II | Ongoing | Heartstring III Proximal Seal System. Intravascular anastomosis occluder. | Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis. | accessdata.fda.gov |
| August 6, 2025 | 97469 | Class II | Ongoing | Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH) System (VH-6000, VH-6001, and VH-6010) is a vessel harvesting kit designed for use wit | Reports of out-of-box failures discovered during the limited launch phase. Failure modes included angled deformity at the attachment site of the Harvesting Tool Jaws and the distal end of the Harvesting Tool Shaft, jaws not fully closed out of box, and heater wire lifted/flexed away from jaws. | accessdata.fda.gov |
| March 20, 2025 | 96439 | Class II | Ongoing | The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm extended length endoscope. The Harvesting Cannula has four lumens which house the endoscope, C-Ring, distal lens | There have been at least 12 complaints from users as of March 3, 2025, reporting that they identified the ceramic C-Ring to be broken in half during use of the device. The ceramic C-Ring has a potential to break while in use. Maquet/Getinge determined that the issue was limited to the units of VH-4000 and VH-4001 manufactured with ceramic C-Ring, and the cer | accessdata.fda.gov |
| March 10, 2025 | 96392 | Class II | Ongoing | Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2). | Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up. | accessdata.fda.gov |
| December 9, 2024 | 95908 | Class I | Ongoing | VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive surgery allowing access for vessel harvesting. | Potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harvesting Tool | accessdata.fda.gov |
| October 16, 2024 | 95614 | Class II | Ongoing | Acrobat-i Positioner. Model Number C-XP-5000Z | Deviations in the manufacturing process created a compromise in the sterile barrier, in which sterility cannot be assured during the duration of the product's 2-year shelf life. | accessdata.fda.gov |
| September 20, 2024 | 95434 | Class I | Ongoing | VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500 | There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use. | accessdata.fda.gov |
| May 31, 2024 | 94802 | Class II | Ongoing | The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens | There were 27 complaints between March 22, 2024, and April 30, 2024, related to VH-3500 and VH-4000, reporting that the C-Ring wire was straightened (due to insufficient bend radius) and that the distance between C-Ring and Harvesting Tool was closer than normal. No adverse events have been reported to date in direct association with this issue. | accessdata.fda.gov |
| May 17, 2024 | 94700 | Class II | Ongoing | The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1. VasoView Hemopro 2, Model Number: VH-4000. 2. VasoView Hemopro 2 with Vasoshield. Model Number: VH-4001. The VASOVIEW HemoPro 2 End | Potential for there to be a fluid ingress into the handle of the harvesting tool, which may lead to the device not providing cautery or providing cautery when not intended. | accessdata.fda.gov |
| December 13, 2023 | 93548 | Class I | Ongoing | Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection | Express chest drains are pre-packaged with sterile water syringes which have bene recalled. If the device is not kept in an upright position, the patient may be exposed to infectious material. Subsequent hazards include but are not limited to infection, abscess, sepsis, and death. | accessdata.fda.gov |
| December 1, 2023 | 93615 | Class II | Ongoing | Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W. | Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may result in polyimide particulate matter being introduced into the arterial conduit for patients undergoing a coronary artery bypass graft (CABG) or peripheral bypass graft surgery. | accessdata.fda.gov |
| October 31, 2023 | 93477 | Class II | Ongoing | Acrobat-i Vacuum Positioner System, Model Number XP-5000Z | The Positioner Arm may not tighten or lock during normal use. | accessdata.fda.gov |
| September 19, 2023 | 93297 | Class II | Ongoing | Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2). | Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device. | accessdata.fda.gov |
| September 13, 2023 | 93085 | Class II | Ongoing | Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a sternotomy incision approach. Product Code: OM-10000Z | Housing Mount Jaw of these devices breaking during normal use and may result in injury to the epicardial tissue or vasculature, or a coronary artery or previously placed bypass graft, or could result in procedural delay and/or conversion. | accessdata.fda.gov |
| June 28, 2023 | 92446 | Class II | Ongoing | ACCESSRAIL Platform (Standard Blade) Part Number SB-1000, and (Deep Blades) Part Number C-DB-1000. Component of a chest stabilization system for cardiac and chest surgery. | The Standard Blade may not securely latch onto the Activator Drive. This may result in the inability to stabilize and position or may result in the loss of stabilization and positioning of heart, release of device component into the patient, and/or a procedural delay and/or conversion. | accessdata.fda.gov |
| March 6, 2023 | 91764 | Class II | Ongoing | VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500 | Some batches of product were not sterilized to their minimum sterilization specification. | accessdata.fda.gov |
| January 30, 2023 | 91671 | Class II | Ongoing | Fusion Bioline Vascular Graft, Part number M00201503046B0 | One (1) Fusion Bioline Vascular graft from lot 25162546, which failed guideline straightness testing, was intermingled with lot 25162549 and distributed to customers. Use of the affected graft may result in reduction of blood flow or unwanted tension causing bleeding and the formation of a pseudo-aneurysm. | accessdata.fda.gov |
| December 22, 2022 | 91363 | Class II | Ongoing | Hemopro 2 with Vasoshield, Model VH-4001 | Ink on the Vasoshield syringe Maquet logo may chip resulting in an unreasonable risk of harm to the patient. Potential harms may include foreign body reaction, coronary embolic event, and peripheral embolic event. | accessdata.fda.gov |
| April 29, 2022 | 90272 | Class II | Terminated | INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurat | Mislabeled: Product labeled as Intergard Woven Straight graft REF IGW0032-30, D: 8 mm, L: 30 cm, contained an Intergard Woven Straight graft of D: 32 mm and L: 30 cm | accessdata.fda.gov |
| February 9, 2022 | 89744 | Class II | Ongoing | Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001. | Potential for corrosion on the pins of the Ultima Activator II Reusable Drive Mechanism. Harms may include allergic reaction, metal toxicity, and other delayed responses. | accessdata.fda.gov |
| January 14, 2022 | 89573 | Class II | Terminated | HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M0020209 | Outer labelling (HEMASHIELD GOLD Knitted Microvel Double Velour Bifurcated Vascular Graft, D: 16 x 8 mm; L: 40 cm) does not correspond to the (inner) sterile packaging labelling (HEMASHIELD GOLD Knitted Microvel Double Velour Straight Vascular Graft, D: 7 mm L: 60 cm). Mislabeled product could cause a disruption of the vascular anastomosis in the long term, | accessdata.fda.gov |
| December 1, 2021 | 89119 | Class II | Terminated | Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890 | There is a probable mislabeling of product. A Hemashield Platinum Woven Double Velour Bifurcated Vasuclar Graft, SN 1259735369, 24 mm x 12 mm, REF Number M00202166241P0 is likely packaged inside of the carton instead of a Hemashield Gold Knitted Microvel Double Velour Bifurcated Vascular Graft; SN 1260004700; 18 mm x 9 mm; REF Number M002020851890 or a Hemas | accessdata.fda.gov |
| April 7, 2020 | 85420 | Class II | Terminated | Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M002020955010 - Product Usage: For use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. | Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts | accessdata.fda.gov |
| April 18, 2019 | 82703 | Class II | Terminated | Maquet Getinge-BEQ-TOP 15800 TUBING PACK Material: 3000065087 | Custom Tubing Sets for Extracorporeal Circulation (ECC)-During sterilization, the closed stopcock/non-vented cap configuration may prevent the flow of humidity/ethylene oxide gas into the fluid-path between the closed port and the non-vented cap therefore the Sterility Assurance Level (SAL) of the stopcock ports cannot be assured | accessdata.fda.gov |
| January 24, 2019 | 82090 | Class II | Terminated | AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site for improved visibility | Potential lack of carbon dioxide (CO2) flow that may result in a procedural delay during off-pump coronary artery bypass (OPCAB). | accessdata.fda.gov |
| January 27, 2017 | 76326 | Class II | Terminated | VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage: The VASOVIEW HEMOPRO VH-3500 is designed for use in conjunction with the 7-mm Endoscope and is intended for specific use with the VASOVIEW HEMOP | Maquet has received several complaints involving the VASOVIEW HEMOPRO VH-3500 which involve the device exhibiting the failure mode of intermittent or no power. | accessdata.fda.gov |
| August 13, 2014 | 69101 | Class II | Terminated | Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump System OM-9000S Axius Xpose 3 Access Device XP-3000 XPOSE 4 Access Device XP-4000 Acrobat V Vacuum Off-Pump System Each Acrobat V Vacuum Off-Pump syst | An internal finding identified the presence of pinholes/cuts in some of the Tyvek pouches of the vacuum tubing sets included as an accessory to Acrobat V Vacuum Off-Pump System, Acrobat SUV Vacuum Off-Pump System, Axius XPOSE 3 Access Device and XPOSE 4 Access Device. | accessdata.fda.gov |
| October 30, 2013 | 66948 | Class II | Terminated | Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular LLC 45 Barbour Pond Drive Wayne, NJ 07470 Indicated for use in minimally invasive surgery allowing access for vessel harvesting and is primarily | Maquet has received an increase in the number of complaints for "self-activated/remains activated/overheats" for the Hemopro VH-30000, "Hemopro 1" | accessdata.fda.gov |
| September 20, 2013 | 66365 | Class II | Terminated | Ultima OPCAB System, Sterile, Rx Only, Product Usage: Intended for use during performance of minimally invasive cardiac surgery through a sternotomy incision approach. The ULTIMA Access RailPlatform in combination with t | MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers OM-2003S & OM-2001D). Labeling for the 2 blade lots had been incorrectly applied. The standard blades from Lot #25052176 were incorrectly labeled as deep blades, and the 20 deep blades from Lot #25052200 were incorrectly labeled as standard blades. | accessdata.fda.gov |
| March 7, 2013 | 64641 | Class II | Terminated | MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version 3.3.0.0) Product Usage: The Cardiohelp System is a blood oxygenation and carbon dioxide removal system used to pump blood through the extracorporeal | It has come to the attention of MAQUET that there have been episodes of brief unexpected shutdown, followed by an automatic device restart of the human machine interface (touch screen) of the CARDIOHELP device. The human machine interface (HMI) is the central display of the CARDIOHELP device, where measured values, settings and alarms are displayed and adjus | accessdata.fda.gov |
| March 27, 2012 | 62121 | Class II | Terminated | CARDIOSAVE Intra-Aortic Balloon Pump An electromechanical system used to inflate and deflate intra-aortic balloons. It provide temporary support to the left ventricle via the principle of counterpulsation. | In the Cardiosave Intra-aortic Balloon Pump, there is a possibility that the coiled cord assembly, a prominent connector cord between the Cardiosave IABP housing and the dual display head which secured atop the IABP may fail as a result of mishandling. | accessdata.fda.gov |
| November 16, 2011 | 60987 | Not yet classified | Terminated | ACROBAT Stabilizers- ACROBAT V Vacuum Off-Pump System (OM-91 OOS), ACROBAT SUV Vacuum Off-Pump System (OM-9000S), ACROBAT Mechanical Off-Pump System (OM-6000S) Product Usage: The OM-9100S Acrobat V Vacuum Off-Pump System | There may be a small perforation in the sterile pouch of select lots of the ACROBAT V, ACROBAT SUV, and ACROBAT Mechanical Stabilizers and the XPOSE 3 and XPOSE 4 Positioners. | accessdata.fda.gov |
| February 23, 2011 | 58053 | Not yet classified | Terminated | Labeling on box reads: MAQUET BEQ-HG 0284 3/8" X 3/8" Connectors, Lot 70041098 but the product packaged inside was MAQUET BEQ-HG 1113 3/16" x 3/16" Connectors, Lot 70041096. The HG 0284 and HG 1113 connectors are package | Tubing connectors incorrectly packaged and labeled. | accessdata.fda.gov |
| December 7, 2010 | 57519 | Not yet classified | Terminated | Hemashield Finesse Ultra-Thin Knitted Cardiovascular Patch Indicated for cardiac and vascular patch grafting. The fabric is recommended for use in patients requiring systemic heparinization prior to, or during, surgery. | One unit of Hemashield Finesse Ultra-thin Knitted Cardiovascular Patch which did not meet the internal release criteria for water permeability was distributed. | accessdata.fda.gov |
| May 24, 2010 | 56004 | Not yet classified | Terminated | Hemashield Gold Woven Double Velour Vascular Branch Graft | Various Hemashield products may develop glycerol droplets on the inner blister of the package if not stored under proper conditions, which could lead to the prolongation of surgery and potentially compromise patient safety. | accessdata.fda.gov |
| May 5, 2010 | 56868 | Not yet classified | Terminated | Maquet Heartstring II Proximal Seal System (HS-1045) manufactured by Maquet Cardiovascular, Wayne, NJ Intended use: medical device for use by cardiac surgeons during CABG procedures to maintain hemostasis and to facilita | Deployment tube may detach during use due to insufficient adhesive, which may result in product failure to operate. | accessdata.fda.gov |
| March 26, 2010 | 55317 | Not yet classified | Terminated | EXXCEL Soft Standard Wall EPTFE Vascular Graft; D:8 mm; L: 50 cm straight. Sterile Intended use: The Standard Wall EXXCEL and EXXCEL Soft ePTFE Vascular Grafts are designed to repair or replace peripheral arteries and to | This is an expansion of Recall # Z-866-2010, adding an additional two lots to the recall of EXXCEL soft Stand Wall EPTFE Vascular Grafts due to a labeling mix up. | accessdata.fda.gov |
| January 20, 2010 | 54355 | Not yet classified | Terminated | EXXCEL Soft Standard Wall EPTFE Vascular Graft; D:8 mm: L: 50 mm straight Maquet Cardiovascular LLS, 45 Barbour Pond Drive, Wayne, NJ 07470 | Labeling mix up: Shelf Carton label for Exxcel Soft Thin Wall Vascular Grafts, lot # 12633379 were mislabeled as Exxcel Soft Standard Wall Grafts. Bleeding could occur if wrong product is used. | accessdata.fda.gov |
| December 17, 2009 | 59865 | Not yet classified | Terminated | VASOVIEW 6 Endoscopic Vessel Harvesting System Manufactured by Maquet Cardiovascular, LLC; 170 Baytech Drive, San Jose, CA 95134. Product Usage: Endoscopic vessel harvesting systems are indicated for use in minimally inv | During routine production quality monitoring process, it was found that UV curing adhesive was not used in a limited number of devices. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Irrigation
- All makers of Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
- All makers of Prosthesis, Vascular Graft, Of Less Then 6mm Diameter
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Instruments, Surgical, Cardiovascular
- All makers of Laparoscope, General & Plastic Surgery
Updated July 15, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.