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Lode B.V. 938902

by Lode B.V.

Lode B.V. 938902 is a cardiopulmonary stress exercise treadmill (FDA Class I; FDA product code IOL, Treadmill, Powered) made by Lode B.V., listed in FDA GUDID since 11 May 2017 (UDI-DI 08717524640156), 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 Number08717524640156 UDI-DI Date11 May 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  • Withdrawn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
Lode B.V.
Generic name
Cardiopulmonary stress exercise treadmill
Model / reference
938902
Primary DI / UDI-DI
08717524640156
FDA product code
IOL
GMDN term
Cardiopulmonary stress exercise treadmill
Device class
Class I
Regulation number
890.5380
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Cardiopulmonary stress exercise treadmill

Similar devices

Other devices filed under FDA product code IOL (TREADMILL, POWERED).

Other devices from Lode B.V.

  • Lode B.V. 965911

    Class II

  • Lode B.V. 965921

    Class II

  • Lode B.V. 967904

    Class II

  • Lode B.V. 960900

    Class II

See all devices from Lode B.V. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)