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Personal Kinetigraph (PKG) GKC-2000

by Gkc Manufacturing Pty Ltd

Personal Kinetigraph (PKG) GKC-2000 is a medical device made by Gkc Manufacturing Pty Ltd, listed in FDA GUDID since 8 Nov 2017 (UDI-DI 09369998107773), 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 Number09369998107773 UDI-DI Date8 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  • Withdrawn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
Personal Kinetigraph (PKG)
Generic name
Neuromuscular motion disorder ambulatory recorder/analyser
Model / reference
GKC-2000
Primary DI / UDI-DI
09369998107773
GMDN term
Neuromuscular motion disorder ambulatory recorder/analyser
GUDID distribution status
In Commercial Distribution

Related devices

Category: Neuromuscular motion disorder ambulatory recorder/analyser

Other devices from Gkc Manufacturing Pty Ltd

See all devices from Gkc Manufacturing Pty Ltd →

Properties

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