meijer

FDA UDI

Class I (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name: meijer FDA UDI
Generic Name: Skin-cover adhesive strip, non-antimicrobial FDA UDI
Device Name: Sheer, Sterile Adhesive Bandages, assorted sizes, 30- 5/8 in x 2 1/4 in (15 mm x 57 mm); 20- 3/4 in x 3 in (19 mm x 76 mm); 10- 1 in x 3 in (25 mm x 76 mm) FDA UDI
Model / Reference: 708820245303 FDA UDI
Description: Sheer, Sterile Adhesive Bandages, assorted sizes, 30- 5/8 in x 2 1/4 in (15 mm x 57 mm); 20- 3/4 in x 3 in (19 mm x 76 mm); 10- 1 in x 3 in (25 mm x 76 mm) FDA UDI

Identifiers

Catalog Number: 2902738 FDA UDI
Primary DI / UDI-DI: 00708820245303 FDA UDI
FDA Product Code: KGX FDA UDI
GMDN Term: Skin-cover adhesive strip, non-antimicrobial FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Skin-cover adhesive strip, non-antimicrobial

meijer by Meijer, 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: Meijer, Inc.

Sources (1)

FDA UDI bd1c0f2b-df11-4c0d-86c4-d2305bf153b2 34 fields · synced Jun 8, 2026