Green Guard CPR Emergency Kit

FDA UDI

Class II (US FDA UDI)

by Greenguard

Identity

Trade Name: Green Guard CPR Emergency Kit FDA UDI
Generic Name: Cardiopulmonary resuscitation mask, single-use FDA UDI
Device Name: Plastic Case attaches to kits and walls. Contains 1 Pair of nitrile gloves, 1 CPR barrier mask and 1 antimicrobial towelette. FDA UDI
Model / Reference: 8070 FDA UDI
Description: Plastic Case attaches to kits and walls. Contains 1 Pair of nitrile gloves, 1 CPR barrier mask and 1 antimicrobial towelette. FDA UDI

Identifiers

Catalog Number: 8070 FDA UDI
Primary DI / UDI-DI: 00347682807009 FDA UDI
510(k) Number: K950769 FDA UDI
FDA Product Code: CBP FDA UDI
GMDN Term: Cardiopulmonary resuscitation mask, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5870 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

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Cardiopulmonary resuscitation mask, single-use

Green Guard CPR Emergency Kit by Greenguard — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K950769 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Greenguard

Sources (1)

FDA UDI 314a20a0-ebe0-402f-ae80-a33ef53e8eca 36 fields · synced May 30, 2026