Remel R21123
by Remel, Inc.
Remel R21123 is a Class I device made by Remel, Inc., listed in FDA GUDID since 3 Jan 2023 (UDI-DI 00848838022630), 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 | Number00848838022630 | Date3 Jan 2023 | StatusListed |
Official records
- AccessGUDID record 00848838022630
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Remel
- Generic name
- Bacterial species differentiation disc IVD
- Model / Ref / Catalog
- R21123
- Primary DI / UDI-DI
- 00848838022630
- FDA product code
- JTO
- GMDN term
- Bacterial species differentiation disc IVD
- Device class
- Class I
- Regulation number
- 866.2660
- GUDID distribution status
- In Commercial Distribution
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