Flushing Medium 10840125M
Flushing Medium 10840125M is an IVF medium (FDA Class II; FDA product code MQL, Media, Reproductive) made by CooperSurgical, Inc., cleared under FDA 510(k) K991327 on 4 May 2000 and listed in FDA GUDID since 4 Feb 2026 (UDI-DI 00888937028577), 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 | Number00888937028577 | Date4 Feb 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK991327 | Date4 May 2000 | StatusActive |
Official records
- AccessGUDID record 00888937028577
- FDA 510(k) database K991327
Across registries
- FDA 510(k) K991327 decided 4 May 2000 Active
- FDA GUDID UDI-DI 00888937028577 listed 4 Feb 2026 Listed
Timeline
- Cleared FDA 510(k) K991327
- Listed FDA GUDID 00888937028577
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Flushing Medium
- Generic name
- IVF medium
- Model / reference
- 10840125M
- Primary DI / UDI-DI
- 00888937028577
- 510(k) Number
- FDA product code
- MQL
- GMDN term
- IVF medium
- Device class
- Class II
- Regulation number
- 884.6180
- GUDID distribution status
- In Commercial Distribution
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