Sil-Select Plus SIP016
by Fertipro NV
Sil-Select Plus SIP016, an IVF medium (FDA Class II; FDA product code MQL, Media, Reproductive) made by Fertipro NV, was cleared under FDA 510(k) K053494 on 23 Mar 2006 and listed in FDA GUDID on 29 Sep 2017 (UDI-DI 54119670001802); the registry lists it as not in commercial distribution (GUDID) 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 | Number54119670001802 | Date29 Sep 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK053494 | Date23 Mar 2006 | StatusActive |
Official records
- AccessGUDID record 54119670001802
- FDA 510(k) database K053494
Across registries
- FDA 510(k) K053494 decided 23 Mar 2006 Active
- FDA GUDID UDI-DI 54119670001802 listed 29 Sep 2017 Listed
Timeline
- Cleared FDA 510(k) K053494
- Listed FDA GUDID 54119670001802
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Sil-Select Plus
- Generic name
- IVF medium
- Model / reference
- SIP016
- Primary DI / UDI-DI
- 54119670001802
- 510(k) Number
- FDA product code
- MQL
- GMDN term
- IVF medium
- Device class
- Class II
- Regulation number
- 884.6180
- GUDID distribution status
- Not in Commercial Distribution
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