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Kroger

FDA UDI

Class I (US FDA UDI)

by Kroger Co., The

Identity

Trade Name
Kroger FDA UDI
Generic Name
Skin-cover adhesive strip, antimicrobial FDA UDI
Device Name
Antibacterial Clear Waterproof Bandages, assorted sizes, 3/4 IN x 1 1/2 IN (19 mm x 38 mm); 3/4 IN x 2 IN (19 mm x 50 mm); 1 IN x 2 1/2 IN (25 mm x 63 mm) FDA UDI
Model / Reference
041260384080 FDA UDI
Description
Antibacterial Clear Waterproof Bandages, assorted sizes, 3/4 IN x 1 1/2 IN (19 mm x 38 mm); 3/4 IN x 2 IN (19 mm x 50 mm); 1 IN x 2 1/2 IN (25 mm x 63 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00041260384080 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

Kroger by Kroger Co., The — 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
Kroger Co., The

Sources (1)

  • FDA UDI f1437566-56b0-47a2-a716-1070e5707c96 34 fields · synced Jun 6, 2026