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Dixieems ZHE920PK

by Wenzhou Caretek Medical Device Co., Ltd.

Dixieems ZHE920PK is a Class II device made by Wenzhou Caretek Medical Device Co., Ltd., listed in FDA GUDID since 23 Mar 2023 (UDI-DI 06975871430109), 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 Number06975871430109 UDI-DI Date23 Mar 2023ListedStatusListed 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  • Withdrawn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
Dixieems
Generic name
Aneroid manual sphygmomanometer
Model / reference
ZHE920PK
Primary DI / UDI-DI
06975871430109
FDA product code
DXQ
GMDN term
Aneroid manual sphygmomanometer
Device class
Class II
Regulation number
870.1120
GUDID distribution status
In Commercial Distribution

Related devices

Category: Aneroid manual sphygmomanometer

Other devices from Wenzhou Caretek Medical Device Co., Ltd.

See all devices from Wenzhou Caretek Medical Device Co., Ltd. →

Properties

  • Lot / batch number
Other properties (14, all answered No)