Rexall DG4345
Rexall DG4345 is a Class I device made by Dolgencorp, LLC, listed in FDA GUDID since 8 Aug 2024 (UDI-DI 00197344110059), 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 | Number00197344110059 | Date8 Aug 2024 | StatusListed |
Official records
- AccessGUDID record 00197344110059
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Rexall
- Generic name
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
- Model / Ref / Catalog
- DG4345
- Primary DI / UDI-DI
- 00197344110059
- FDA product code
- LZA
- GMDN term
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
- Device class
- Class I
- Regulation number
- 880.6250
- GUDID distribution status
- In Commercial Distribution
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