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Haier Biomedical HXC-1369B

by Qingdao Haier Biomedical Co Ltd

Haier Biomedical HXC-1369B is a Class II device made by Qingdao Haier Biomedical Co Ltd, listed in FDA GUDID since 26 Oct 2026 (UDI-DI 06949573505298), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06949573505298 UDI-DI Date26 Oct 2026ListedStatusListed 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  • Withdrawn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
Haier Biomedical
Generic name
Blood refrigerator
Model / reference
HXC-1369B
Primary DI / UDI-DI
06949573505298
FDA product code
KSE
GMDN term
Blood refrigerator
Device class
Class II
Regulation number
864.9700
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KSE (Refrigerator, Freezer, Blood Storage).

Other devices from Qingdao Haier Biomedical Co Ltd

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)