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Redicare

FDA UDI

Class I (US FDA UDI)

by Redicare Llc

Identity

Trade Name
Redicare FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
50 Fabric Wide Strip Bandages Latex Free Heavy Weight Wound Protection 50/box FDA UDI
Model / Reference
Fabric Wide Strip Bandage FDA UDI
Description
50 Fabric Wide Strip Bandages Latex Free Heavy Weight Wound Protection 50/box FDA UDI

Identifiers

Catalog Number
0103004 FDA UDI
Primary DI / UDI-DI
B70901030041 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Adhesive bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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: Adhesive bandage

Redicare by Redicare Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Adhesive bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Redicare Llc

Sources (1)

  • FDA UDI 7ef60c84-2e62-41eb-95cb-6a36209e4fda 35 fields · synced Jun 8, 2026