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Meridian Viral Transport

FDA UDI

Class I (US FDA UDI)

by Meridian Bioscience, Inc.

Identity

Trade Name
Meridian Viral Transport FDA UDI
Generic Name
General specimen collection kit IVD, clinical FDA UDI
Device Name
Meridian Viral Transport is a system which contains all materials necessary to collect and transport clinical specimens for viral isolation. FDA UDI
Model / Reference
505021 FDA UDI
Description
Meridian Viral Transport is a system which contains all materials necessary to collect and transport clinical specimens for viral isolation. FDA UDI

Identifiers

Catalog Number
505021 FDA UDI
Primary DI / UDI-DI
00840733101410 FDA UDI
510(k) Number
K853500 FDA UDI
FDA Product Code
JSM 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
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

Yes

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: General specimen collection kit IVD, clinical

Meridian Viral Transport by Meridian Bioscience, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen collection kit IVD, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6f79fdd6-e93f-4a70-a03e-d3b286b94dc1 37 fields · synced Jun 1, 2026