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Xenon Master

FDA UDI

Class I (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
Drierite, Indicating Blue/White Blend, Plastic Jar, 1 Lb. for Xenon Administration System FDA UDI
Model / Reference
MN0028 FDA UDI
Description
Drierite, Indicating Blue/White Blend, Plastic Jar, 1 Lb. for Xenon Administration System FDA UDI

Identifiers

Primary DI / UDI-DI
00850022357817 FDA UDI
FDA Product Code
CBL FDA UDI
GMDN Term
Xenon administration system, diagnostic x-ray/CT FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Xenon Master by Medi Nuclear Corp., Inc. — Class I — 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 75b04067-01cf-4739-b7ca-993e9f874147 35 fields · synced Jun 8, 2026