LiquiPhil™ TLP260
LiquiPhil™ TLP260 is a Class I device made by Providus Holdings, Inc., listed in FDA GUDID since 7 May 2024 (UDI-DI 00812266030772), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00812266030772 | Date7 May 2024 | StatusListed |
Official records
- AccessGUDID record 00812266030772
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- LiquiPhil™
- Generic name
- MRI phantom, test object
- Model / Ref / Catalog
- TLP260
- Primary DI / UDI-DI
- 00812266030772
- FDA product code
- IXG
- GMDN term
- MRI phantom, test object
- Device class
- Class I
- Regulation number
- 892.1950
- GUDID distribution status
- In Commercial Distribution
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