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MN0002

by Medi Nuclear Corp., Inc.

MN0002 is a xenon administration system (FDA Class I; FDA product code CBL, Absorbent, Carbon-Dioxide) made by Medi Nuclear Corp., Inc., listed in FDA GUDID since 9 Nov 2020 (UDI-DI 00850022357152), 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 Number00850022357152 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  • Withdrawn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

Generic name
Xenon administration system, diagnostic x-ray/CT
Model / reference
MN0002
Description
Soda Lime, Plastic Container, 1 Lb for Xenon Administration System
Primary DI / UDI-DI
00850022357152
FDA product code
CBL
GMDN term
Xenon administration system, diagnostic x-ray/CT
Device class
Class I
Regulation number
868.5300
GUDID distribution status
In Commercial Distribution

Related devices

Category: Xenon administration system, diagnostic x-ray/CT

Similar devices

Other devices filed under FDA product code CBL (Absorbent, Carbon-Dioxide).

Other devices from Medi Nuclear Corp., Inc.

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

Properties

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