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Haier Biomedical DW-30L698

by Qingdao Haier Biomedical Co Ltd

Haier Biomedical DW-30L698 is a Class II device made by Qingdao Haier Biomedical Co Ltd, listed in FDA GUDID since 11 Aug 2026 (UDI-DI 06949573500132), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06949573500132 UDI-DI Date11 Aug 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  • Withdrawn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 plasma freezer
Model / reference
DW-30L698
Primary DI / UDI-DI
06949573500132
FDA product code
KSE
GMDN term
Blood plasma freezer
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)