microMend PRO

FDA UDI

Class I (US FDA UDI)

by Kitotech Medical Inc

Identity

Trade Name: microMend PRO FDA UDI
Generic Name: Skin-closure adhesive strip FDA UDI
Device Name: Skin Closure Devices: Medium - 12 mm x 28 mm (2 Closures per Pouch) FDA UDI
Model / Reference: MM01SM2 FDA UDI
Description: Skin Closure Devices: Medium - 12 mm x 28 mm (2 Closures per Pouch) FDA UDI

Identifiers

Catalog Number: MM01SM2 FDA UDI
Primary DI / UDI-DI: 00850018777322 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

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

Category: Skin-closure adhesive strip

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

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3M™ Steri-Strip™ — 3M COMPANY · Class I
CareOne — Ahold U.S.A., Inc. · Class I
DeRoyal — DEROYAL INDUSTRIES, INC. · Class I

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 0a822ce4-8308-4e85-a64c-2b1abed6ef4d 36 fields · synced Jun 8, 2026