Kromopan KRM001
by Lascod Spa
Kromopan KRM001 is a Class II device made by Lascod Spa, listed in FDA GUDID since 15 Sep 2017 (UDI-DI 18016200010328), 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 | Number18016200010328 | Date15 Sep 2017 | StatusListed |
Official records
- AccessGUDID record 18016200010328
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Kromopan
- Generic name
- Alginate dental impression material
- Model / reference
- KRM001
- Primary DI / UDI-DI
- 18016200010328
- FDA product code
- ELW
- GMDN term
- Alginate dental impression material
- Device class
- Class II
- Regulation number
- 872.3660
- GUDID distribution status
- In Commercial Distribution
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