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MedSource Yankaeur Tip & Tube, Non-Vented

FDA UDI

Class II (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Yankaeur Tip & Tube, Non-Vented FDA UDI
Generic Name
Electron beam sterilizer FDA UDI
Device Name
MedSource Yankaeur Tip & Tube, Non-Vented FDA UDI
Model / Reference
MS-YK50 FDA UDI
Description
MedSource Yankaeur Tip & Tube, Non-Vented FDA UDI

Identifiers

Primary DI / UDI-DI
00816703021972 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Electron beam sterilizer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Electron beam sterilizer

MedSource Yankaeur Tip & Tube, Non-Vented by Medsource International Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electron beam sterilizer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medsource International Llc

Sources (1)

  • FDA UDI 90aff324-cb86-4f3a-ab56-4db9056ff4a4 33 fields · synced Jun 8, 2026