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G.00

by Philips Medical Systems Hsg

G.00 is a Class II device made by Philips Medical Systems Hsg, listed in FDA GUDID since 14 Oct 2016 (UDI-DI 00884838033672), 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 Number00884838033672 UDI-DI Date14 Oct 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  • Withdrawn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
Medical equipment clinical data interfacing software
Model / reference
G.00
Primary DI / UDI-DI
00884838033672
FDA product code
DXJ
GMDN term
Medical equipment clinical data interfacing software
Device class
Class II
Regulation number
870.2450
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical equipment clinical data interfacing software

Similar devices in this category

Other devices filed under Medical equipment clinical data interfacing software.

Other devices from Philips Medical Systems Hsg

See all devices from Philips Medical Systems Hsg →

Properties

  • Lot / batch number
Other properties (14, all answered No)