Mastisol 1
by Ferndale Laboratories, Inc. 4 variants
Mastisol 1 (0523-15) is a Class I device made by Ferndale Laboratories, Inc., listed in FDA GUDID since 19 Sep 2022 (UDI-DI 00304960523150), 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 | Number00304960523150 | Date19 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 00304960523150
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mastisol
- Generic name
- Skin surface device adhesive, sterile
- Model / Ref / Catalog
- 1, 0523-15
- Primary DI / UDI-DI
- 00304960523150
- FDA product code
- KGX
- GMDN term
- Skin surface device adhesive, sterile
- Device class
- Class I
- Regulation number
- 880.5240
- GUDID distribution status
- In Commercial Distribution
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