BandGrip® Micro-Anchor® Skin Closure

FDA UDI

Class I (US FDA UDI)

by Bandgrip Inc.

Identity

Trade Name: BandGrip® Micro-Anchor® Skin Closure FDA UDI
Generic Name: Skin-closure adhesive strip FDA UDI
Device Name: 3.8 cm x 8.8 cm, 1 closure/pouch FDA UDI
Model / Reference: BG1002 FDA UDI
Description: 3.8 cm x 8.8 cm, 1 closure/pouch FDA UDI

Identifiers

Catalog Number: BG1002 FDA UDI
Primary DI / UDI-DI: 00850010207100 FDA UDI
FDA Product Code: KGX FDA UDI
MKY FDA UDI
GDT FDA UDI
FZQ FDA UDI
GMDN Term: Skin-closure adhesive strip FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5240 FDA UDI
878.4320 FDA UDI
878.4760 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

Sterilization Method

Radiation Sterilization FDA UDI

Dimensions & Sizes

Size: Width — 8.8 Centimeter FDA UDI
Length — 3.8 Centimeter FDA UDI

Category: Skin-closure adhesive strip

BandGrip® Micro-Anchor® Skin Closure by Bandgrip Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-closure adhesive strip.

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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: Bandgrip Inc.

Sources (1)

FDA UDI c0bce48a-b5af-493c-8faf-2429a19da1d6 36 fields · synced Jun 1, 2026