Micromat® 3105-M-B
by Pmt Corp.
Micromat® 3105-M-B is a Class II device made by Pmt Corp., cleared under FDA 510(k) K831117 on 30 May 1984 and listed in FDA GUDID since 1 May 2026 (UDI-DI 00650551005896), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00650551005896 | Date1 May 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK831117 | Date30 May 1984 | StatusActive |
Official records
- AccessGUDID record 00650551005896
- FDA 510(k) database K831117
Across registries
- FDA 510(k) K831117 decided 30 May 1984 Active
- FDA GUDID UDI-DI 00650551005896 listed 1 May 2026 Listed
Timeline
- Cleared FDA 510(k) K831117
- Listed FDA GUDID 00650551005896
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Micromat®
- Generic name
- Surgical capillary wound drain, non-luminal
- Model / reference
- 3105-M-B
- Primary DI / UDI-DI
- 00650551005896
- 510(k) Number
- FDA product code
- KKX, FNW
- GMDN term
- Surgical capillary wound drain, non-luminal
- Device class
- Class II
- Regulation number
- 878.4370
- GUDID distribution status
- In Commercial Distribution
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