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RTgo

by Philips Oy

RTgo (459801266633) is a Class II device made by Philips Oy, listed in FDA GUDID since 7 Jun 2019 (UDI-DI 00884838092112), 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 Number00884838092112 UDI-DI Date7 Jun 2019ListedStatusListed 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  • Withdrawn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
MRI system application software
Model / Ref / Catalog
RTgo, 459801266633
Primary DI / UDI-DI
00884838092112
FDA product code
MUJ
GMDN term
MRI system application software
Device class
Class II
Regulation number
892.5050
GUDID distribution status
In Commercial Distribution

Related devices

Category: MRI system application software

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Properties

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