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Redicare

FDA UDI

Class II (US FDA UDI)

by Redicare Llc

Identity

Trade Name
Redicare FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Device Name
Kit to assist with basic Body Fluids cleanup intended for use at general workplaces. Typically found by a first aid kit for use in the cleanup of blood or other bodily fluids. FDA UDI
Model / Reference
Blood-Borne Pathogens Kit FDA UDI
Description
Kit to assist with basic Body Fluids cleanup intended for use at general workplaces. Typically found by a first aid kit for use in the cleanup of blood or other bodily fluids. FDA UDI

Identifiers

Catalog Number
0115009 FDA UDI
Primary DI / UDI-DI
B70901150090 FDA UDI
FDA Product Code
OKG FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

Yes

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: First aid kit, medicated

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

Similar devices

Also classified as First aid kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Redicare Llc

Sources (1)

  • FDA UDI 2616f7f6-2125-41c8-b58c-bb33d5b048fb 35 fields · synced May 30, 2026