Data / Medical devices / China / Zhejiang Chimin Tang Medicine Trade Co., Ltd.
Zhejiang Chimin Tang Medicine Trade Co., Ltd.: FDA-registered device maker in Taizhou Zhejiang, China, 6 510(k) clearances
Zhejiang Chimin Tang Medicine Trade Co., Ltd. is registered with the FDA (registration 3020294761) in Taizhou Zhejiang, China. It lists 3 device types. The FDA files 6 510(k) clearances under its listings, the newest dated April 9, 2021. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3020294761
- Address
- 888 Beiyuan Road, Huangyan, Taizhou Zhejiang, China, 318020
- Owner or operator
- Zhejiang Chimin Tang Medicine Trade Co., Ltd. (10082349)
- Roles
- Exporter to the US
- First device listed
- July 14, 2021
- Registered through
- 2026
- Brand names listed
- Easypoint, Vanishpoint
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 2 | Exporter to the US | accessdata.fda.gov |
| Syringe, Antistick | MEG | 2 | Exporter to the US | accessdata.fda.gov |
| Tubes, Vials, Systems, Serum Separators, Blood Collection | JKA | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| April 9, 2021 | K202325 | EasyPoint Blood Collection Plus | JKA | Substantially Equivalent | Retractable Technologies, Inc. | accessdata.fda.gov |
| June 17, 2014 | K133635 | EASYPOINT NEEDLE | FMI | Substantially Equivalent | Retractable Technologies, Inc. | accessdata.fda.gov |
| February 12, 1998 | K980069 | VANISHPOINT SYRINGE | MEG | Substantially Equivalent | Retractable Technologies, Inc. | accessdata.fda.gov |
| November 7, 1997 | K973301 | ANTI-STICK SYRINGE WITH INTEGRAL HYPODERMIC NEEDLE/VANISHPOINT SYRINGE | MEG | Substantially Equivalent | Retractable Technologies, Inc. | accessdata.fda.gov |
| May 29, 1997 | K970803 | ANTI-STICK SYRINGE WITH INTEGRAL HYPODERMIC NEEDLE VANISHPOINT SYRINGE | MEG | Substantially Equivalent | Retractable Technologies, Inc. | accessdata.fda.gov |
| December 28, 1995 | K946219 | POP-N-LOK SYRINGE | MEG | Substantially Equivalent | Retractable Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Antistick
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
Updated April 9, 2021. 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.