Data / Medical devices / China / ShanDong WeiGao Group Medical Polymer Co., Ltd
ShanDong WeiGao Group Medical Polymer Co., Ltd: FDA-registered device maker in Weihai Shandong, China, 1 510(k) clearance
ShanDong WeiGao Group Medical Polymer Co., Ltd is registered with the FDA (registration 3007084575) in Weihai Shandong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 23, 2009. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3007084575
- Address
- No.1 Weigao Road, Torch Hi-tech Science Park, Weihai Shandong, China, 264210
- Owner or operator
- Weigao Group Company Limited (10025293)
- Roles
- Contract manufacturer, Contract sterilizer, Manufacturer
- First device listed
- June 13, 2008
- Registered through
- 2026
- Brand names listed
- Disposable Angiographic Syringes, Nipro Syringe, ORAL/ENTERAL SYRINGE, Patient Safe Luer Cap, Patient Safety Syringe, Sterile High Pressure Angiographic Syringes for Single Use
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Injector And Syringe, Angiographic | DXT | 2 | Contract manufacturer, Contract sterilizer, Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Contract manufacturer, Contract sterilizer | accessdata.fda.gov |
| Tube, Feeding | FPD | 2 | Contract manufacturer, Contract sterilizer | 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 |
|---|---|---|---|---|---|---|
| March 23, 2009 | K082439 | DISPOSABLE ANGIOGRAPHIC SYRINGE, MODEL(S) CT-200-NE, CT-200-MA, CT-200+200-MA, CT-200-LF, CT -100-NE, CT-200NE, CT-50+CT | DXT | Substantially Equivalent | Shandong Weigao Medical Polymer Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Tube, Feeding
- All makers of Injector And Syringe, Angiographic
Updated March 23, 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.