Data / Medical devices / China / Yangzhou Weideli Trading Co., Ltd.
Yangzhou Weideli Trading Co., Ltd.: FDA-registered device maker in Yangzhou Jiangsu, China, 5 510(k) clearances
Yangzhou Weideli Trading Co., Ltd. is registered with the FDA (registration 3008808123) in Yangzhou Jiangsu, China. It lists 10 device types. The FDA files 5 510(k) clearances under its listings, the newest dated June 9, 2023. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3008808123
- Address
- RM 2412, Building 5 Cai Fu Plaza 287 Yangzijiang Middle Rd, Yangzhou Jiangsu, China, 225009
- Owner or operator
- Yangzhou Weideli Trading Co., Ltd. (10034893)
- Roles
- Contract manufacturer, Repackager or relabeler, Specification developer
- First device listed
- January 13, 2011
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Contract manufacturer | accessdata.fda.gov |
| Container, I.V. | KPE | 2 | Specification developer | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Specification developer | accessdata.fda.gov |
| Gown, Examination | FME | 1 | Specification developer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Specification developer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Specification developer | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Specification developer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Repackager or relabeler | accessdata.fda.gov |
| System/Device, Pharmacy Compounding | NEP | 2 | Specification developer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 2 | 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 |
|---|---|---|---|---|---|---|
| June 9, 2023 | K230992 | DJF Intravascular Administration Set | FPA | Substantially Equivalent | Yangzhou Wei DE LI Trade Co., Ltd. | accessdata.fda.gov |
| July 21, 2022 | K220184 | Pump Alignment Syringe | FMF | Substantially Equivalent | Jiangsu Caina Medical Co.,Ltd | accessdata.fda.gov |
| December 19, 2012 | K121803 | INTRAVASCULAR ADMINISTRATION SET | FPA | Substantially Equivalent | Acta Medical, LLC | accessdata.fda.gov |
| July 13, 2012 | K121161 | EMPTY EVA SOLUTION CONTAINER EMPTY EVA DUAL CHAMBER SOLUTION CONTAINER | KPE | Substantially Equivalent | Acta Medical, LLC | accessdata.fda.gov |
| March 29, 2012 | K112863 | ENTERAL ADMINISTRATION SET WITH SOLUTION CONTAINER, ENTERAL ADMINISTRATION SET, ENTERAL EXTENSION SET WITH MINITUBE CONN | KNT | Substantially Equivalent | Acta Medical, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Tubes, Gastrointestinal (And Accessories)
- All makers of Set, Administration, Intravascular
- All makers of Gown, Examination
- All makers of Container, I.V.
- All makers of Dispenser, Liquid Medication
- All makers of System/Device, Pharmacy Compounding
Updated June 9, 2023. 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.