Cramer Blister Derm 030905
Cramer Blister Derm 030905 is a Class I device made by Cramer Products, Inc., listed in FDA GUDID since 1 Oct 2018 (UDI-DI 00311960560610), 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 | Number00311960560610 | Date1 Oct 2018 | StatusListed |
Official records
- AccessGUDID record 00311960560610
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Cramer Blister Derm
- Generic name
- Wound hydrogel dressing, non-sterile
- Model / reference
- 030905
- Primary DI / UDI-DI
- 00311960560610
- FDA product code
- NAE
- GMDN term
- Wound hydrogel dressing, non-sterile
- Device class
- Class I
- Regulation number
- 878.4022
- GUDID distribution status
- In Commercial Distribution
- Size
- Circumference — 3 Inch
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