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Jg-900P

by Nihon Kohden America, Inc.

Jg-900P is a Class II device made by Nihon Kohden America, Inc., listed in FDA GUDID since 19 Sep 2016 (UDI-DI 00841983100673), 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 Number00841983100673 UDI-DI Date19 Sep 2016ListedStatusListed 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  • Withdrawn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

Generic name
Carbon dioxide monitor
Model / Ref / Catalog
JG-900P
Primary DI / UDI-DI
00841983100673
FDA product code
CCK, MHX
GMDN term
Carbon dioxide monitor
Device class
Class II
Regulation number
868.1400, 870.1025
GUDID distribution status
In Commercial Distribution

Related devices

Category: Carbon dioxide monitor

Similar devices

Also classified as Carbon dioxide monitor.

Other devices from Nihon Kohden America, Inc.

See all devices from Nihon Kohden America, Inc. →

Properties

  • Prescription use
Other properties (14, all answered No)