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Redicare

FDA UDI

Class I (US FDA UDI)

by Redicare Llc

Identity

Trade Name
Redicare FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
10 Sterile Gauze Pads 3x3 inch 10/box FDA UDI
Model / Reference
Sterile Pads 3" x 3" FDA UDI
Description
10 Sterile Gauze Pads 3x3 inch 10/box FDA UDI

Identifiers

Catalog Number
0104025 FDA UDI
Primary DI / UDI-DI
B70901040251 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Woven gauze pad, non-antimicrobial

Redicare by Redicare Llc — 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

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Manufacturer

Manufacturer
Redicare Llc

Sources (1)

  • FDA UDI 01d6fb05-2366-459c-b064-bfab19a1be7f 35 fields · synced May 30, 2026