ResQGARD MP KIT

FDA UDI

Class II (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name: ResQGARD MP KIT FDA UDI
Generic Name: Demand valve FDA UDI
Device Name: RESQGARD MP KIT FDA UDI
Model / Reference: 12-2387-030 FDA UDI
Description: RESQGARD MP KIT FDA UDI

Identifiers

Primary DI / UDI-DI: 00847946045326 FDA UDI
FDA Product Code: BWF FDA UDI
JOW FDA UDI
GMDN Term: Demand valve FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5690 FDA UDI
870.5800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

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

FDA UDI

Manufacturing Date

FDA UDI

Category: Demand valve

ResQGARD MP KIT by Zoll Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Zoll Medical Corporation

Sources (1)

FDA UDI 2ac8e55a-8add-4f64-ba94-78dc53200432 34 fields · synced Jun 8, 2026