SynVitro Flush 15840125D
by Origio A/S
SynVitro Flush 15840125D is an IVF medium (FDA Class II; FDA product code MQL, Media, Reproductive) made by Origio A/S, cleared under FDA 510(k) K003163 on 22 Mar 2001 and listed in FDA GUDID since 22 Jun 2016 (UDI-DI 00888937801903), 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 | Number00888937801903 | Date22 Jun 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK003163 | Date22 Mar 2001 | StatusActive |
Official records
- AccessGUDID record 00888937801903
- FDA 510(k) database K003163
Across registries
- FDA 510(k) K003163 decided 22 Mar 2001 Active
- FDA GUDID UDI-DI 00888937801903 listed 22 Jun 2016 Listed
Timeline
- Cleared FDA 510(k) K003163
- Listed FDA GUDID 00888937801903
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SynVitro Flush
- Generic name
- IVF medium
- Model / reference
- 15840125D
- Primary DI / UDI-DI
- 00888937801903
- 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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