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Hokanson TMC7

by D. E. Hokanson, Inc.

Hokanson TMC7 (03701), a blood pressure cuff (FDA Class II; FDA product code DXQ, Blood Pressure Cuff) made by D. E. Hokanson, Inc., was listed in FDA GUDID on 9 Sep 2016 (UDI-DI 00817065020474); the registry lists it as not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00817065020474 UDI-DI Date9 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Hokanson
Generic name
Blood pressure cuff, reusable
Model / Ref / Catalog
TMC7, 03701
Primary DI / UDI-DI
00817065020474
FDA product code
DXQ
GMDN term
Blood pressure cuff, reusable
Device class
Class II
Regulation number
870.1120
GUDID distribution status
Not in Commercial Distribution
Size
Width — 7 Centimeter

Similar devices

Other devices filed under FDA product code DXQ (Blood Pressure Cuff).

Other devices from D. E. Hokanson, Inc.

See all devices from D. E. Hokanson, Inc. →

Properties

  • Premarket exempt
  • Manufacturing date
Other properties (13, all answered No)