Remel R40235
by Remel, Inc.
Remel R40235 is a Class I device made by Remel, Inc., listed in FDA GUDID since 23 Dec 2022 (UDI-DI 00848838066115), 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 | Number00848838066115 | Date23 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 00848838066115
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Remel
- Generic name
- Biological stain IVD
- Model / Ref / Catalog
- R40235
- Primary DI / UDI-DI
- 00848838066115
- FDA product code
- HYI
- GMDN term
- Biological stain IVD
- Device class
- Class I
- Regulation number
- 864.1850
- GUDID distribution status
- In Commercial Distribution
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