caina 22Gx1 1/4"
by Jiangsu Caina Medical Co., Ltd
caina 22Gx1 1/4" (BC062230-W) is a Class II device made by Jiangsu Caina Medical Co., Ltd, cleared under FDA 510(k) K200027 on 9 Sep 2020 and listed in FDA GUDID since 14 May 2025 (UDI-DI 16971564462324), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number16971564462324 | Date14 May 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK200027 | Date9 Sep 2020 | StatusActive |
Official records
- AccessGUDID record 16971564462324
- FDA 510(k) database K200027
Across registries
- FDA 510(k) K200027 decided 9 Sep 2020 Active
- FDA GUDID UDI-DI 16971564462324 listed 14 May 2025 Listed
Timeline
- Cleared FDA 510(k) K200027
- Listed FDA GUDID 16971564462324
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- caina
- Generic name
- Blood collection tube holder/needle
- Model / Ref / Catalog
- 22Gx1 1/4", BC062230-W
- Primary DI / UDI-DI
- 16971564462324
- 510(k) Number
- FDA product code
- JKA, FMI
- GMDN term
- Blood collection tube holder/needle
- Device class
- Class II
- Regulation number
- 862.1675, 880.5570
- GUDID distribution status
- In Commercial Distribution
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