Vial Assembly 900
Vial Assembly 900 is a Class II device made by Paragon Vision Sciences, listed in FDA GUDID since 8 Dec 2017 (UDI-DI B222900), 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 | NumberB222900 | Date8 Dec 2017 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vial Assembly
- Generic name
- Contact lens case
- Model / reference
- 900
- Primary DI / UDI-DI
- B222900
- FDA product code
- LRX
- GMDN term
- Contact lens case
- Device class
- Class II
- Regulation number
- 886.5928
- GUDID distribution status
- In Commercial Distribution
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