Cradle, Sonalis 210222
by Best Nomos
Cradle, Sonalis 210222 is a Class I device made by Best Nomos, cleared under FDA 510(k) K973786 on 2 Jan 1998 and listed in FDA GUDID since 31 Oct 2016 (UDI-DI 00852656007151), active as of 22 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 | Number00852656007151 | Date31 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK973786 | Date2 Jan 1998 | StatusActive |
Official records
- AccessGUDID record 00852656007151
- FDA 510(k) database K973786
Across registries
- FDA 510(k) K973786 decided 2 Jan 1998 Active
- FDA GUDID UDI-DI 00852656007151 listed 31 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K973786
- Listed FDA GUDID 00852656007151
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Cradle, Sonalis
- Generic name
- Medical table clamp
- Model / reference
- 210222
- Primary DI / UDI-DI
- 00852656007151
- 510(k) Number
- FDA product code
- IWJ
- GMDN term
- Medical table clamp
- Device class
- Class I
- Regulation number
- 892.5650
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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