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ReeVue 8100

by Korr Medical Technologies Inc.

ReeVue 8100 is a Class II device made by Korr Medical Technologies Inc., listed in FDA GUDID since 3 Mar 2022 (UDI-DI B6568100), 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 NumberB6568100 UDI-DI Date3 Mar 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
ReeVue
Generic name
Indirect calorimeter
Model / reference
8100
Primary DI / UDI-DI
B6568100
FDA product code
BZL
GMDN term
Indirect calorimeter
Device class
Class II
Regulation number
868.1730
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code BZL (Computer, Oxygen-Uptake).

Other devices from Korr Medical Technologies Inc.

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)