Ultracell® S90900
by Beaver-Visitec International Inc
Ultracell® S90900 is a Class II device made by Beaver-Visitec International Inc, listed in FDA GUDID since 27 Jun 2024 (UDI-DI 30886158012086), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number30886158012086 | Date27 Jun 2024 | StatusListed |
Official records
- AccessGUDID record 30886158012086
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ultracell®
- Generic name
- Medical device cleaning sponge/set
- Model / Ref / Catalog
- S90900
- Description
- 'INSTRUMENT WIPE, FOIL POUCHED 3'' X 3'' X 2MM (300/SP)'
- Primary DI / UDI-DI
- 30886158012086
- FDA product code
- HOZ
- GMDN term
- Medical device cleaning sponge/set
- Device class
- Class II
- Regulation number
- 886.4790
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Radiation Sterilization
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