OneTouch Verio Flex 024-395
by Lifescan Europe Switzerland GUDID
Product code NBW
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00353885013017 | Date1 Sep 2026 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- OneTouch Verio Flex
- Generic Name
- Glucose monitoring system IVD, home-use
- Model / Reference
- 024-395
- Primary DI / UDI-DI
- 00353885013017
- FDA Product Code
- NBW, LFR
- GMDN Term
- Glucose monitoring system IVD, home-use
- Device Class
- Class II
- Regulation Number
- 862.1345
- Commercial Distribution
- In Commercial Distribution
Other devices from Lifescan Europe
Properties & raw data
Show properties, registry sources and raw records
Other properties (9)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 1795c632-1df6-41ea-862f-cb161bd61b24