Customed 712057052781
Customed 712057052781 (9002781) is a Class II device made by Customed, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI M20890027810), registry data as of 23 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 | NumberM20890027810 | Date23 Sep 2016 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Customed
- Generic name
- Sputum specimen container IVD
- Model / Ref / Catalog
- 712057052781, 9002781
- Primary DI / UDI-DI
- M20890027810
- FDA product code
- BYZ
- GMDN term
- Sputum specimen container IVD
- Device class
- Class II
- Regulation number
- 880.6740
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 80 Milliliter
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