Micromat®

FDA UDI

Class II (US FDA UDI)

by Pmt Corp.

Identity

Trade Name: MICROMAT® FDA UDI
Generic Name: Surgical capillary wound drain, non-luminal FDA UDI
Device Name: 3 FRENCH MICROSURGICAL GRID W/SUCTION-BLUE BACKGROUND-W/OUT WIRE FDA UDI
Model / Reference: 3103-3G-B-WO FDA UDI
Description: 3 FRENCH MICROSURGICAL GRID W/SUCTION-BLUE BACKGROUND-W/OUT WIRE FDA UDI

Identifiers

Primary DI / UDI-DI: 00650551096153 FDA UDI
510(k) Number: K831117 FDA UDI
FDA Product Code: KKX FDA UDI
GMDN Term: Surgical capillary wound drain, non-luminal FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4370 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical capillary wound drain, non-luminal

Micromat® by Pmt Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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MICROMAT® — Pmt Corp. · Class II

Cleared under the same submission

K831117 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Pmt Corp.

Sources (1)

FDA UDI ae18e1a7-0c04-42e9-98ab-e3c22aaa09f4 34 fields · synced Jun 8, 2026