Monoject 8881601600
Monoject 8881601600 is a Class II device made by Cardinal Health 200, LLC, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 30884521015054), 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 | Number30884521015054 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 30884521015054
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Monoject
- Generic name
- Insulin syringe/needle, basic
- Model / Ref / Catalog
- 8881601600
- Primary DI / UDI-DI
- 30884521015054
- FDA product code
- FMF
- GMDN term
- Insulin syringe/needle, basic
- Device class
- Class II
- Regulation number
- 880.5860
- GUDID distribution status
- In Commercial Distribution
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