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Lifesaver

FDA UDI

Class II (US FDA UDI)

by GaleMed Xiamen Co., Ltd.

Identity

Trade Name
LIFESAVER FDA UDI
Generic Name
Pulmonary resuscitator, manual, reusable FDA UDI
Device Name
MANUAL RESUSCITATOR,DURABLE INFANT W/MASK FDA UDI
Model / Reference
HD-5347 FDA UDI
Description
MANUAL RESUSCITATOR,DURABLE INFANT W/MASK FDA UDI

Identifiers

Catalog Number
5347 FDA UDI
Primary DI / UDI-DI
24710810093238 FDA UDI
FDA Product Code
BTM FDA UDI
GMDN Term
Pulmonary resuscitator, manual, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5915 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulmonary resuscitator, manual, reusable

Lifesaver by GaleMed Xiamen Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary resuscitator, manual, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 613c6cf0-93b9-4e3e-a94a-d98ea167a91f 35 fields · synced Jun 7, 2026