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MR-RT RT CouchTop XD

by Philips Oy

MR-RT RT CouchTop XD (989603083751) is a Class II device made by Philips Oy, listed in FDA GUDID since 31 Aug 2022 (UDI-DI 00884838103528), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00884838103528 UDI-DI Date31 Aug 2022ListedStatusListed GUDID: not 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  • Withdrawn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
MR-Rt
Generic name
Radiation therapy treatment planning positioning kit
Model / Ref / Catalog
RT CouchTop XD, 989603083751
Primary DI / UDI-DI
00884838103528
FDA product code
MUJ
GMDN term
Radiation therapy treatment planning positioning kit
Device class
Class II
Regulation number
892.5050
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code MUJ (System, Planning, Radiation Therapy Treatment).

Other devices from Philips Oy

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Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)