URIVerse™ W095
URIVerse™ W095 is a Class I device made by Copan Wasp Srl, listed in FDA GUDID since 20 Oct 2023 (UDI-DI 58059796361700), 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 | Number58059796361700 | Date20 Oct 2023 | StatusListed |
Official records
- AccessGUDID record 58059796361700
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- URIVerse™
- Generic name
- Pipetting system IVD
- Model / Ref / Catalog
- W095
- Primary DI / UDI-DI
- 58059796361700
- FDA product code
- JQW
- GMDN term
- Pipetting system IVD
- Device class
- Class I
- Regulation number
- 862.2750
- GUDID distribution status
- In Commercial Distribution
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