Marketlab Inc 5688
Marketlab Inc 5688 is a Class II device made by Marketlab Inc., listed in FDA GUDID since 16 Nov 2018 (UDI-DI 00817517020533), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00817517020533 | Date16 Nov 2018 | StatusListed |
Official records
- AccessGUDID record 00817517020533
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Marketlab Inc
- Generic name
- Blood collection tube spike syringe adaptor
- Model / Ref / Catalog
- 5688
- Primary DI / UDI-DI
- 00817517020533
- FDA product code
- JKA
- GMDN term
- Blood collection tube spike syringe adaptor
- Device class
- Class II
- Regulation number
- 862.1675
- GUDID distribution status
- In Commercial Distribution
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