Data / Medical devices / Mexico / Productos Para El Cuidado De La Salud
Productos Para El Cuidado De La Salud: FDA-registered device maker in NOGALES Sonora, Mexico, 9 510(k) clearances
Productos Para El Cuidado De La Salud is registered with the FDA (registration 9611590) in NOGALES Sonora, Mexico. It lists 61 device types. The FDA files 9 510(k) clearances under its listings, the newest dated May 29, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 9611590
- FEI number
- 1000237915
- Address
- CARRETERA INTERNACIONAL KM. 6.5 Terrazas Del Cid, NOGALES Sonora, Mexico, 84000
- Owner or operator
- C. R. Bard, Inc. (2212754)
- Roles
- Contract manufacturer, Repackager or relabeler
- First device listed
- March 18, 1994
- Registered through
- 2027
- Brand names listed
- "J" Guidewires, & Foley Tray (I.C.), (Tieman Model) Coude Tip, 100cc Silicone Evacuator, 3-spring Y-connector, 30cc Balloon w/o Catheter, 4 - CHANNEL MONITOR W, 4 Channel Monitor w/ Uroflow and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Accessories, Catheter, G-U | KNY | 2 | Repackager or relabeler | accessdata.fda.gov |
| Adaptor, Catheter | GCE | 1 | Contract manufacturer | accessdata.fda.gov |
| Adaptor, Ureteral Catheter | EYI | 1 | Contract manufacturer | accessdata.fda.gov |
| Apparatus, Suction, Single Patient Use, Portable, Nonpowered | GCY | 1 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Bag, Bile Collecting | EXF | 2 | Contract manufacturer | accessdata.fda.gov |
| Bag, Urine Collection, Leg, For External Use, Non-Sterile | NNW | 1 | Contract manufacturer | accessdata.fda.gov |
| Bag, Urine Collection, Leg, For External Use, Sterile | FAQ | 1 | Contract manufacturer | accessdata.fda.gov |
| Basin, Emesis | FNY | 1 | Contract manufacturer | accessdata.fda.gov |
| Biliary Catheter For Irrigation And Contrast Injection, Exempt | PTT | 2 | Repackager or relabeler | accessdata.fda.gov |
| Cannula And Trocar, Suprapubic, Non-Disposable | FBM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Catheter, Coude | EZC | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Irrigation | GBX | 1 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Catheter, Malecot | FEW | 2 | Repackager or relabeler | accessdata.fda.gov |
| Catheter, Retention Type, Balloon | EZL | 2 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Catheter, Straight | EZD | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Ureteral, Gastro-Urology | EYB | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Urethral | GBM | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Urological | KOD | 2 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Catheter, Urological (Antimicrobial) And Accessories | MJC | 2 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Catheter, Ventricular, General & Plastic Surgery | GBS | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Clamp, Penile | FHA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Collector, Ostomy | EXB | 1 | Contract manufacturer | accessdata.fda.gov |
| Collector, Urine, (And Accessories) For Indwelling Catheter | KNX | 2 | Contract manufacturer | accessdata.fda.gov |
| Collector, Urine, Pediatric, For Indwelling Catheter | FFH | 2 | Contract manufacturer | accessdata.fda.gov |
| Collector, Urine, Powered, Non Indwelling Catheter | NZU | 1 | Contract manufacturer | accessdata.fda.gov |
| Connector, Catheter | GCD | 1 | Contract manufacturer | accessdata.fda.gov |
| Container, Liquid Medication, Graduated | KYW | 1 | Contract manufacturer | accessdata.fda.gov |
| Container, Specimen, Non-Sterile | NNI | 1 | Contract manufacturer | accessdata.fda.gov |
| Device, Cystometric, Hydraulic | FEN | 2 | Contract manufacturer | accessdata.fda.gov |
| Device, Intravascular Catheter Securement | KMK | 1 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Device, Urine Flow Rate Measuring, Non-Electrical, Disposable | FFG | 2 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Dilator, Urethral | KOE | 2 | Repackager or relabeler | accessdata.fda.gov |
| Dislodger, Stone, Basket, Ureteral, Metal | FFL | 2 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Dress, Surgical | FYE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Electrode, Electrosurgical, Active, Urological | FAS | 2 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Endoscopic Access Overtube, Gastroenterology-Urology | FED | 2 | Repackager or relabeler | accessdata.fda.gov |
| Endoscopic Irrigation/Suction System | OCX | 2 | Contract manufacturer | accessdata.fda.gov |
| Evacuator, Gastro-Urology | KQT | 2 | Contract manufacturer | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Forceps | HTD | 1 | Contract manufacturer | accessdata.fda.gov |
| Hemostatic Wound Dressing Without Thrombin Or Other Biologics | QSY | U | Repackager or relabeler | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | Contract manufacturer | accessdata.fda.gov |
| Intra-Abdominal Pressure Monitoring Device | PHU | U | Contract manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Contract manufacturer | accessdata.fda.gov |
| Sound, Urethral, Metal Or Plastic | FBX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Stent, Ureteral | FAD | 2 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Stylet For Catheter, Gastro-Urology | EZB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Suprapubic Catheter Accessories | QGC | 1 | Contract manufacturer | accessdata.fda.gov |
| Surgical Instruments, G-U, Manual (And Accessories) | KOA | 1 | Contract manufacturer | accessdata.fda.gov |
| System, Thermal Regulating | DWJ | 2 | Contract manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) | FCM | 2 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Tube, Double Lumen For Intestinal Decompression And/Or Intubation | FEG | 2 | Contract manufacturer | accessdata.fda.gov |
| Tube, Nasogastric | BSS | 2 | Contract manufacturer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 2 | Contract manufacturer | accessdata.fda.gov |
| Urine Collection Kit (Excludes Hiv Testing) | OIE | 1 | Contract manufacturer | accessdata.fda.gov |
| Urinometer, Electrical | EXS | 2 | Repackager or relabeler | accessdata.fda.gov |
| Urinometer, Mechanical | EXR | 2 | Contract manufacturer | accessdata.fda.gov |
| Uroflowmeter | EXY | 2 | Repackager or relabeler | 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 |
|---|
| May 29, 2026 | K254076 | BD Touchless Plus Unisex Pre-Lubricated Urethral Catheter Kit | FCM | Unknown | C.R. Bard, Inc. | accessdata.fda.gov |
| August 21, 2012 | K121485 | GUARDIVA ANTIMICROBIAL HAEMSTATIC IV DRESSING | QSY | Substantially Equivalent | Hemcon Medical Technologies Europe, Ltd. | accessdata.fda.gov |
| April 24, 2007 | K070879 | BARD MALECOT AND PEZZER DRAINS | FEW | Substantially Equivalent | C.R. Bard, Inc. | accessdata.fda.gov |
| December 7, 2004 | K043193 | BARD INLAYOPTIMA URETERAL STENT WITH SUTURE | FAD | Substantially Equivalent | C.R. Bard, Inc. | accessdata.fda.gov |
| December 30, 2003 | K033778 | MODIFICATION TO BARD AQUAGUIDE URETERAL CONDUIT | FED | Substantially Equivalent | C.R. Bard, Inc. | accessdata.fda.gov |
| May 19, 2000 | K000723 | HYDROPHILIC SILICONE FOLEY CATHETER AND PERSONAL CATHETER (HYDROPHILIC AND NON-HYDROPHILIC) | KOD | Substantially Equivalent | Rochester Medical Corp. | accessdata.fda.gov |
| December 15, 1998 | K983498 | BARD INLAY LUBRICIOUS DOUBLE PIGTAIL URETERAL STENT WITH SUTURE (HEREINAFTER REFERRED TO AS BARD LUBRICIOUS URETERAL STE | FAD | Substantially Equivalent | C.R. Bard, Inc. | accessdata.fda.gov |
| December 17, 1996 | K962538 | BARD COAGULATING RESECTOR MODEL (3552XX; XX=01,02,03,04,05 OR 06) | FAS | Substantially Equivalent | C.R. Bard, Inc. | accessdata.fda.gov |
| April 30, 1991 | K903345 | BARD (R) LUBRICIOUS - COATED URETERAL STENT SUTURE | FAD | Substantially Equivalent | C.R. Bard, Inc. | accessdata.fda.gov |
Compare with other makers
Updated May 29, 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.