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Xenon Master Administration Set

FDA UDI

Class II (US FDA UDI)

by Medi Nuclear Corp., Inc.

Identity

Trade Name
Xenon Master Administration Set FDA UDI
Generic Name
Straight/elbow breathing circuit connector, single-use FDA UDI
Device Name
Xenon Administration Set: Tube, HEPA Filter and face mask with adapter FDA UDI
Model / Reference
MN2891M FDA UDI
Description
Xenon Administration Set: Tube, HEPA Filter and face mask with adapter FDA UDI

Identifiers

Primary DI / UDI-DI
00850022357138 FDA UDI
FDA Product Code
IYT FDA UDI
GMDN Term
Straight/elbow breathing circuit connector, single-use 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

Yes

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: Straight/elbow breathing circuit connector, single-use

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

Similar devices

Also classified as Straight/elbow breathing circuit connector, single-use.

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 137b4a4a-f63d-43b3-8a45-4d0774287b3d 35 fields · synced Jun 8, 2026