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Xenon Master XE-104-2

by Medi Nuclear Corp., Inc.

Xenon Master XE-104-2 is a xenon administration system (FDA Class II; FDA product code IYT, System, Rebreathing, Radionuclide) made by Medi Nuclear Corp., Inc., listed in FDA GUDID since 9 Nov 2020 (UDI-DI 00850022357244), 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 Number00850022357244 UDI-DI Date9 Nov 2020ListedStatusListed 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  • Withdrawn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
Xenon Master
Generic name
Xenon administration system, diagnostic x-ray/CT
Model / reference
XE-104-2
Primary DI / UDI-DI
00850022357244
FDA product code
IYT
GMDN term
Xenon administration system, diagnostic x-ray/CT
Device class
Class II
Regulation number
892.1390
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IYT (System, Rebreathing, Radionuclide).

Other devices from Medi Nuclear Corp., Inc.

See all devices from Medi Nuclear Corp., Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)