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TEVADAPTOR® Spike Port Adaptor

FDA UDI

Class II (US FDA UDI)

by Teva Pharmaceutical Industries Limited

Identity

Trade Name
TEVADAPTOR® Spike Port Adaptor FDA UDI
Generic Name
Medication transfer set FDA UDI
Device Name
TEVADAPTOR® Spike Port Adaptor for use with OnGuardTM contained Medication System FDA UDI
Model / Reference
MG412113 FDA UDI
Description
TEVADAPTOR® Spike Port Adaptor for use with OnGuardTM contained Medication System FDA UDI

Identifiers

Catalog Number
MG412113 FDA UDI
Primary DI / UDI-DI
27298119121137 FDA UDI
510(k) Number
K141448 FDA UDI
FDA Product Code
ONB FDA UDI
GMDN Term
Medication transfer set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medication transfer set

TEVADAPTOR® Spike Port Adaptor by Teva Pharmaceutical Industries Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medication transfer set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e08d31db-2957-4853-af79-0c4f36ef15da 35 fields · synced May 30, 2026