microMend

FDA UDI

Class I (US FDA UDI)

by Kitotech Medical Inc

Identity

Trade Name: microMend FDA UDI
Generic Name: Skin-closure adhesive strip FDA UDI
Device Name: Emergency Laceration Closures (Qty. 5), VARIETY: 1 Pack of 2 SMALL 1/4 IN x 1 IN (7 mm x 28 mm); 1 Pack of 2 MEDIUM 1/2 IN x 1 IN (12 mm x 28 mm); 1 ONE 1 IN x 1 IN (25 mm x 28mm) FDA UDI
Model / Reference: MSXWD004 FDA UDI
Description: Emergency Laceration Closures (Qty. 5), VARIETY: 1 Pack of 2 SMALL 1/4 IN x 1 IN (7 mm x 28 mm); 1 Pack of 2 MEDIUM 1/2 IN x 1 IN (12 mm x 28 mm); 1 ONE 1 IN x 1 IN (25 mm x 28mm) FDA UDI

Identifiers

Catalog Number: MSXWD004 FDA UDI
Primary DI / UDI-DI: 00850018777261 FDA UDI
FDA Product Code: GDT FDA UDI
KGX FDA UDI
GMDN Term: Skin-closure adhesive strip FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4760 FDA UDI
880.5240 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

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Skin-closure adhesive strip

microMend by Kitotech Medical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Kitotech Medical Inc

Sources (1)

FDA UDI 8b3e4828-b370-48d8-a129-2116fe4422b0 36 fields · synced Jun 1, 2026