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Mingwei MWHX7420B

by MingWei Medical Technology(Suzhou)Co., LTD

Mingwei MWHX7420B is a Class I device made by MingWei Medical Technology(Suzhou)Co., LTD, listed in FDA GUDID since 30 Dec 2020 (UDI-DI 26973915530185), 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 Number26973915530185 UDI-DI Date30 Dec 2020ListedStatusListed 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  • Withdrawn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
Mingwei
Generic name
X-ray tube housing assembly, diagnostic
Model / reference
MWHX7420B
Primary DI / UDI-DI
26973915530185
FDA product code
ITY
GMDN term
X-ray tube housing assembly, diagnostic
Device class
Class I
Regulation number
892.1760
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ITY (Assembly, Tube Housing, X-Ray, Diagnostic).

Other devices from MingWei Medical Technology(Suzhou)Co., LTD

See all devices from MingWei Medical Technology(Suzhou)Co., LTD →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)