Ceros RM-DC0212805
Ceros RM-DC0212805 is a Class II device made by Rhino Medical Supply Inc, listed in FDA GUDID since 15 Mar 2024 (UDI-DI 00850060997082), registry data as of 22 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 | Number00850060997082 | Date15 Mar 2024 | StatusListed |
Official records
- AccessGUDID record 00850060997082
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ceros
- Generic name
- Insulin syringe/needle, basic
- Model / Ref / Catalog
- RM-DC0212805
- Primary DI / UDI-DI
- 00850060997082
- FDA product code
- FMF, FMI
- GMDN term
- Insulin syringe/needle, basic
- Device class
- Class II
- Regulation number
- 880.5860, 880.5570
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 1.0 MilliliterNeedle Gauge — 28 GaugeLength — .5 Inch
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