← Back to catalogue

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
Decorated unicorn bandages, Sterile Adhesive Bandages, Antibacterial Pads, all one size, 3/4 x 3 in FDA UDI
Model / Reference
713733521697 FDA UDI
Description
Decorated unicorn bandages, Sterile Adhesive Bandages, Antibacterial Pads, all one size, 3/4 x 3 in FDA UDI

Identifiers

Catalog Number
4212610 FDA UDI
Primary DI / UDI-DI
00713733521697 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
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI ea22364f-ca4e-4da3-bca3-78402593d7f7 35 fields · synced Jun 1, 2026