Medline OTCM170100
Medline OTCM170100 is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 1 Dec 2022 (UDI-DI 10193489084795), 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 | Number10193489084795 | Date1 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 10193489084795
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Medline
- Generic name
- Wart-removal cryogenic kit
- Model / Ref / Catalog
- OTCM170100
- Primary DI / UDI-DI
- 10193489084795
- FDA product code
- GEH
- GMDN term
- Wart-removal cryogenic kit
- Device class
- Class II
- Regulation number
- 878.4350
- GUDID distribution status
- In Commercial Distribution
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