Data / Medical devices / China / Anhui Kangda Medical Products Co., Ltd.
Anhui Kangda Medical Products Co., Ltd.: FDA-registered device maker in Tianchang City Anhui, China, 2 510(k) clearances
Anhui Kangda Medical Products Co., Ltd. is registered with the FDA (registration 3003310007) in Tianchang City Anhui, China. It lists 7 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 2, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003310007
- Address
- No.88 Zhenxing Road, Yangcun Town, Tianchang City Anhui, China, 239304
- Owner or operator
- ANHUI KANGDA MEDICAL PRODUCTS CO., LTD. (9057034)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- May 2, 2005
- Registered through
- 2026
- Brand names listed
- BAIXIN BLOOD COLLECTION SET, BAIXIN DENTAL NEEDLE, BAIXIN SYRINGES AND HYPODERMIC NEEDLES, BLUNT FILL NEEDLE, Baixin, MN Health Inc
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dispenser, Liquid Medication | KYX | 1 | Contract manufacturer | accessdata.fda.gov |
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Needle, Dental | DZM | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Contract manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Manufacturer | accessdata.fda.gov |
| Tube, Collection, Capillary Blood | GIO | 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 |
|---|---|---|---|---|---|---|
| July 2, 2009 | K083686 | BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES | FMF | Substantially Equivalent | Anhui Kangda Medical Products Co., Ltd. | accessdata.fda.gov |
| June 11, 2009 | K083687 | BAIXIN INTRAVASCULAR ADMINISTRATION SET | FPA | Substantially Equivalent | Anhui Kangda Medical Products Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Tube, Collection, Capillary Blood
- All makers of Needle, Aspiration And Injection, Disposable
- All makers of Syringe, Piston
- All makers of Set, Administration, Intravascular
- All makers of Dispenser, Liquid Medication
- All makers of Needle, Dental
Updated July 2, 2009. 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.