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Meijer

FDA UDI

Class I (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
Meijer FDA UDI
Generic Name
Skin-cover adhesive strip, antimicrobial FDA UDI
Device Name
Antibacterial Flexible Fabric Sterile Adhesive Bandages, all one size, 3/4 IN x 3 IN (19 mm x 76 mm) FDA UDI
Model / Reference
719283746597 FDA UDI
Description
Antibacterial Flexible Fabric Sterile Adhesive Bandages, all one size, 3/4 IN x 3 IN (19 mm x 76 mm) FDA UDI

Identifiers

Catalog Number
4692194 FDA UDI
Primary DI / UDI-DI
00719283746597 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Skin-cover adhesive strip, 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin-cover adhesive strip, antimicrobial

Meijer by Meijer, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-cover adhesive strip, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI 648311ea-e264-407c-9e85-145d7886be64 34 fields · synced Jun 1, 2026