3M™ Coban™ 2082S
by 3M Company
3M™ Coban™ 2082S is a Class I device made by 3M Company, listed in FDA GUDID since 5 Feb 2021 (UDI-DI 00707387802318), 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 | Number00707387802318 | Date5 Feb 2021 | StatusListed |
Official records
- AccessGUDID record 00707387802318
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- 3M™ Coban™
- Generic name
- Pressure bandage, non-latex, single-use
- Model / Ref / Catalog
- 2082S
- Primary DI / UDI-DI
- 00707387802318
- FDA product code
- FQM
- GMDN term
- Pressure bandage, non-latex, single-use
- Device class
- Class I
- Regulation number
- 880.5075
- GUDID distribution status
- In Commercial Distribution
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