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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
Moisture Absorbing Granule Cartridge, Disposable, (Drierite) FDA UDI
Model / Reference
MN2772 FDA UDI
Description
Moisture Absorbing Granule Cartridge, Disposable, (Drierite) FDA UDI

Identifiers

Primary DI / UDI-DI
00850022357794 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

Yes

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 b9b7f926-6794-4d7c-9d39-dc6e6a5a47c4 35 fields · synced Jun 6, 2026