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Xenon Master

FDA UDI

Class II (US FDA UDI)

by Medi Nuclear Corp., Inc.

Identity

Trade Name
Xenon Master FDA UDI
Generic Name
Xenon administration system, diagnostic x-ray/CT FDA UDI
Device Name
C02 Absorbing Granule Cartridge, Disposable, (Soda Lime) FDA UDI
Model / Reference
MN2773 FDA UDI
Description
C02 Absorbing Granule Cartridge, Disposable, (Soda Lime) FDA UDI

Identifiers

Primary DI / UDI-DI
00850022357800 FDA UDI
FDA Product Code
IYT FDA UDI
GMDN Term
Xenon administration system, diagnostic x-ray/CT FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1390 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Xenon Master by Medi Nuclear Corp., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Xenon administration system, diagnostic x-ray/CT.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medi Nuclear Corp., Inc.

Sources (1)

  • FDA UDI 8055a8fe-30ad-446d-bb47-fb5e50db1622 35 fields · synced May 30, 2026