Unolok+ 19 G X ¾"
by Hindustan Syringes and Medical Devices Limited
Unolok+ 19 G X ¾" (00233) is a Class II device made by Hindustan Syringes and Medical Devices Limited, cleared under FDA 510(k) K000592 on 12 Apr 2001 and listed in FDA GUDID since 26 Apr 2017 (UDI-DI 08903347002336), 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 | Number08903347002336 | Date26 Apr 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK000592 | Date12 Apr 2001 | StatusActive |
Official records
- AccessGUDID record 08903347002336
- FDA 510(k) database K000592
Across registries
- FDA 510(k) K000592 decided 12 Apr 2001 Active
- FDA GUDID UDI-DI 08903347002336 listed 26 Apr 2017 Listed
Timeline
- Cleared FDA 510(k) K000592
- Listed FDA GUDID 08903347002336
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Unolok+
- Generic name
- Venous butterfly needle/set
- Model / Ref / Catalog
- 19 G X ¾", 00233
- Description
- UNOLOK+ Luer Lock Infusion Set,19 G X ¾" ( 1.10X19MM) 7" TUBE MYCO RE-ORDER # 7001P-19L
- Primary DI / UDI-DI
- 08903347002336
- 510(k) Number
- FDA product code
- FPA
- GMDN term
- Venous butterfly needle/set
- Device class
- Class II
- Regulation number
- 880.5440
- GUDID distribution status
- In Commercial Distribution
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