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Kroger

FDA UDI

Class U (US FDA UDI)

by Kroger Co., The

Identity

Trade Name
Kroger FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, antimicrobial FDA UDI
Device Name
Antibacterial Non-Stick Pads, all one size, 3 IN x 4 IN (76 mm x 101 mm). Contains: Polyhexamethylene Biguadine (PHMB) 0.2% FDA UDI
Model / Reference
041260377501 FDA UDI
Description
Antibacterial Non-Stick Pads, all one size, 3 IN x 4 IN (76 mm x 101 mm). Contains: Polyhexamethylene Biguadine (PHMB) 0.2% FDA UDI

Identifiers

Primary DI / UDI-DI
00041260377501 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, antimicrobial FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound-nonadherent dressing, absorbent, antimicrobial

Kroger by Kroger Co., The — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, absorbent, antimicrobial.

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 f5c32d77-da13-4970-9f01-5cd821b0d5e0 34 fields · synced May 30, 2026