← Back to catalogue

AllCare

FDA UDI

Class I (US FDA UDI)

by Allcare, Inc.

Identity

Trade Name
AllCare FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
SPONGE GAUZE 4X4IN 12PLY, 100% COTTON, 10/PK NON-STERILE FDA UDI
Model / Reference
AG4412 FDA UDI
Description
SPONGE GAUZE 4X4IN 12PLY, 100% COTTON, 10/PK NON-STERILE FDA UDI

Identifiers

Catalog Number
AG4412 FDA UDI
Primary DI / UDI-DI
10182921000127 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze pad, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Category: Woven gauze pad, non-antimicrobial

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

Similar devices

Also classified as Woven gauze pad, non-antimicrobial.

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
Allcare, Inc.

Sources (1)

  • FDA UDI 8a303a37-37ed-4200-a07f-f109ca94d5a3 36 fields · synced May 30, 2026