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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, non-antimicrobial FDA UDI
Device Name
Smart-Flex, Sterile Adhesive Bandages, assorted sizes FDA UDI
Model / Reference
713733521598 FDA UDI
Description
Smart-Flex, Sterile Adhesive Bandages, assorted sizes FDA UDI

Identifiers

Catalog Number
4212588 FDA UDI
Primary DI / UDI-DI
00713733521598 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
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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 28 Millimeter FDA UDI
Width — 22 Millimeter FDA UDI
Width — 15 Millimeter 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

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI ef547e2d-6d0d-4e76-b332-9a1933f66e7c 36 fields · synced May 30, 2026