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ERGOMETER ergoselect 4 M 191001

by ergoline GmbH

ERGOMETER ergoselect 4 M 191001 is a Class II device made by ergoline GmbH, listed in FDA GUDID since 20 Nov 2017 (UDI-DI 04059358001586), 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 Number04059358001586 UDI-DI Date20 Nov 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  • Withdrawn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
ERGOMETER ergoselect 4 M
Generic name
Bicycle ergometer
Model / reference
191001
Primary DI / UDI-DI
04059358001586
FDA product code
ISD
GMDN term
Bicycle ergometer
Device class
Class II
Regulation number
890.5360
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ISD (Exerciser, Measuring).

Other devices from ergoline GmbH

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)