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Discovery PETCT 710

by GE Medical Systems, L.L.C.

Discovery PETCT 710 is a Class II device made by GE Medical Systems, L.L.C., listed in FDA GUDID since 1 Aug 2016 (UDI-DI 00840682102995), 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 Number00840682102995 UDI-DI Date1 Aug 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  • Withdrawn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

Trade name
Discovery
Generic name
Full-body CT system
Model / reference
PETCT 710
Primary DI / UDI-DI
00840682102995
FDA product code
KPS
GMDN term
Full-body CT system
Device class
Class II
Regulation number
892.1200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Full-body CT systemPET system

Similar devices

Other devices filed under FDA product code KPS (System, tomography, computed, emission).

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Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)