Skip to content

Lifesaver Hd-5342

by GaleMed Xiamen Co., Ltd.

Lifesaver Hd-5342 is a Class II device made by GaleMed Xiamen Co., Ltd., listed in FDA GUDID since 28 Sep 2016 (UDI-DI 24710810093207), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number24710810093207 UDI-DI Date28 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Lifesaver
Generic name
Pulmonary resuscitator, manual, reusable
Model / Ref / Catalog
HD-5342, 5342
Primary DI / UDI-DI
24710810093207
FDA product code
BTM
GMDN term
Pulmonary resuscitator, manual, reusable
Device class
Class II
Regulation number
868.5915
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code BTM (Ventilator, Emergency, Manual (Resuscitator)).

Other devices from GaleMed (Xiamen) Co., Ltd.

See all devices from GaleMed (Xiamen) Co., Ltd. →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)