OneTouch Ultra Plus 024-272
OneTouch Ultra Plus 024-272 is a Class II device made by Lifescan Europe, listed in FDA GUDID since 31 Aug 2022 (UDI-DI 00353885012645), registry data as of 23 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 | Number00353885012645 | Date31 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 00353885012645
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- OneTouch Ultra Plus
- Generic name
- Glucose IVD, control
- Model / reference
- 024-272
- Primary DI / UDI-DI
- 00353885012645
- FDA product code
- NBW, LFR
- GMDN term
- Glucose IVD, control
- Device class
- Class II
- Regulation number
- 862.1345
- GUDID distribution status
- In Commercial Distribution
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