Redicare

FDA UDI

Class I (US FDA UDI)

by Redicare Llc

Identity

Trade Name: Redicare FDA UDI
Generic Name: Cardiopulmonary resuscitation kit, single-use FDA UDI
Device Name: Resuscitation Kit in a plastic container containing masks and gloves for performing cardiopulmonary resuscitation (CPR). FDA UDI
Model / Reference: Resuscitation Kit FDA UDI
Description: Resuscitation Kit in a plastic container containing masks and gloves for performing cardiopulmonary resuscitation (CPR). FDA UDI

Identifiers

Catalog Number: 0102018 FDA UDI
Primary DI / UDI-DI: B70901020180 FDA UDI
FDA Product Code: OHO FDA UDI
GMDN Term: Cardiopulmonary resuscitation kit, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Cardiopulmonary resuscitation kit, single-use

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

Similar devices

Also classified as Cardiopulmonary resuscitation kit, single-use.

Ambu® SPUR® II Adult Resuscitator — Ambu A/S · Class II
Ambu® SPUR® II Pediatric Resuscitator — Ambu A/S · Class II
Ever Ready First Aid — XIAMEN COMPOWER MEDICAL TECH. CO., LTD
Ambu® SPUR® II Adult Resuscitator — Ambu A/S · Class II
Aquatic Solutions — XIAMEN COMPOWER MEDICAL TECH. CO., LTD
Compower — XIAMEN COMPOWER MEDICAL TECH. CO., LTD
BROSELOW™ — Airlife, Inc. · Class II
Ambu® SPUR® II Adult Resuscitator — Ambu A/S · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Redicare Llc

Sources (1)

FDA UDI ae0192d4-d1bc-400c-8ef4-1551f4381f0e 34 fields · synced Jun 1, 2026