Data / Medical devices / China / Shaoxing Haitech Medical Products Co., Ltd
Shaoxing Haitech Medical Products Co., Ltd: FDA-registered device maker in SHAOXING Zhejiang, China, 1 510(k) clearance
Shaoxing Haitech Medical Products Co., Ltd is registered with the FDA (registration 3010889742) in SHAOXING Zhejiang, China. It lists 13 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 15, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010889742
- Address
- No.201, Building 4, 1423 Renmin East Road, SHAOXING Zhejiang, China, 312035
- Owner or operator
- Shaoxing Haitech Medical Products Co., Ltd (10046508)
- Roles
- Manufacturer
- First device listed
- March 31, 2014
- Registered through
- 2026
- Brand names listed
- 1810001, 1810002, 7880550.10A; 7880550.12A; 7880550.14A; 7880550.16A, 880501; 880504; 880508, 880522; 880523; 880524; 880525; 880526; 880527; 880543, 880536; 880537; 880538; 880539; 880540; 880541, 880541, 880541TS; 880541TM; 880541TL; 880541TXL and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Airway, Oropharyngeal, Anesthesiology | CAE | 1 | Manufacturer | accessdata.fda.gov |
| Cannula, Nasal, Oxygen | CAT | 1 | Manufacturer | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Manufacturer | accessdata.fda.gov |
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Manufacturer | accessdata.fda.gov |
| Condenser, Heat And Moisture (Artificial Nose) | BYD | 1 | Manufacturer | accessdata.fda.gov |
| Device, Fixation, Tracheal Tube | CBH | 1 | Manufacturer | accessdata.fda.gov |
| Device, Rebreathing | BYW | 1 | Manufacturer | accessdata.fda.gov |
| Filter, Bacterial, Breathing-Circuit | CAH | 2 | Manufacturer | accessdata.fda.gov |
| Mask, Gas, Anesthetic | BSJ | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Oxygen, Low Concentration, Venturi | BYF | 1 | Manufacturer | accessdata.fda.gov |
| Staple, Removable (Skin) | GDT | 1 | Manufacturer | accessdata.fda.gov |
| Support, Breathing Tube | JAY | 1 | Manufacturer | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| February 15, 2024 | K222917 | Breathing circuit bacterial/viral filter | CAH | Substantially Equivalent | Shaoxing Haitech Medical Products Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Irrigating (Non Dental)
- All makers of Device, Rebreathing
- All makers of Condenser, Heat And Moisture (Artificial Nose)
- All makers of Cannula, Nasal, Oxygen
- All makers of Staple, Removable (Skin)
- All makers of Mask, Oxygen, Low Concentration, Venturi
Updated February 15, 2024. 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.