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Hokanson 43476

by D. E. Hokanson, Inc.

Hokanson 43476 is a Class II device made by D. E. Hokanson, Inc., listed in FDA GUDID since 18 Jul 2017 (UDI-DI 00817065022089), 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 Number00817065022089 UDI-DI Date18 Jul 2017ListedStatusListed 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  • Withdrawn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
Hokanson
Generic name
Blood pressure cuff, reusable
Model / Ref / Catalog
43476
Primary DI / UDI-DI
00817065022089
FDA product code
DXQ
GMDN term
Blood pressure cuff, reusable
Device class
Class II
Regulation number
870.1120
GUDID distribution status
In Commercial Distribution
Size
Width — 12 Centimeter

Related devices

Category: Blood pressure cuff, reusable

Similar devices in this category

Other devices filed under Blood pressure cuff, reusable.

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)