Viral Transport Media (VTM) 3ml

FDA UDI

Class I (US FDA UDI)

by A. L. B. Luz

Identity

Trade Name: Viral Transport Media (VTM) 3ml FDA UDI
Generic Name: General specimen collection kit IVD, clinical FDA UDI
Device Name: The ALB Luz Viral Transport Media is intended for the collection and transport of upper respiratory clinical specimens containing Influenza A, Influenza B, Respiratory Syncytial Virus (RSV), and Rhinovirus from the collection site to the testing laboratory. The Viral Transport Media is a culture-based media that is intended to be used with standard diagnostic/identification techniques that utilize stable recoverable infectious viral particles. FDA UDI
Model / Reference: MEI00175 FDA UDI
Description: The ALB Luz Viral Transport Media is intended for the collection and transport of upper respiratory clinical specimens containing Influenza A, Influenza B, Respiratory Syncytial Virus (RSV), and Rhinovirus from the collection site to the testing laboratory. The Viral Transport Media is a culture-based media that is intended to be used with standard diagnostic/identification techniques that utilize stable recoverable infectious viral particles. FDA UDI

Identifiers

Catalog Number: MEI00175 FDA UDI
Primary DI / UDI-DI: 07898996204631 FDA UDI
FDA Product Code: JSM FDA UDI
LIO FDA UDI
GMDN Term: General specimen collection kit IVD, clinical FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 866.2390 FDA UDI
866.2900 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General specimen collection kit IVD, clinical

Viral Transport Media (VTM) 3ml by A. L. B. Luz — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: A. L. B. Luz

Sources (1)

FDA UDI 1b02ebd9-c511-49f1-b07a-6a72fc136d98 34 fields · synced May 30, 2026