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: MICROSURGICAL GRID WITH SUCTION - BLUE BACKGROUND - WITHOUT WIRE FDA UDI
Model / Reference: 3103-5G-WO FDA UDI
Description: MICROSURGICAL GRID WITH SUCTION - BLUE BACKGROUND - WITHOUT WIRE FDA UDI

Identifiers

Catalog Number: 3103-5G-WO FDA UDI
Primary DI / UDI-DI: 00650551037712 FDA UDI
FDA Product Code: KKX FDA UDI
FNW 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 5 French 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

Similar devices

Also classified as Surgical capillary wound drain, non-luminal.

Front1 Health Partners — DEGANIA SILICONE LTD · Class I
Front1 Health Partners — DEGANIA SILICONE LTD · Class I
Front1 Health Partners — DEGANIA SILICONE LTD · Class I
WIKI Drain, 15 Fr, 3 cm, 1 Drain — TOOLS FOR SURGERY, LLC · Class I
Front1 Health Partners — DEGANIA SILICONE LTD · Class I
WIKI Drain, 15 Fr, 3 cm, 6 Drains — TOOLS FOR SURGERY, LLC · Class I
Front1 Health Partners — DEGANIA SILICONE LTD · Class I
MICROMAT® — Pmt Corp. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Pmt Corp.

Sources (1)

FDA UDI e7edfcc8-8c93-44e4-817f-936c460ca50b 37 fields · synced Jun 8, 2026