← Back to catalogue

BD™ Universal Viral Transport for Viral, Specimens

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD™ Universal Viral Transport for Viral, Specimens FDA UDI
Generic Name
General specimen container IVD, additive/medium FDA UDI
Device Name
Vial Universal Viral Transport FDA UDI
Model / Reference
220220 FDA UDI
Description
Vial Universal Viral Transport FDA UDI

Identifiers

Catalog Number
220220 FDA UDI
Primary DI / UDI-DI
30382902202203 FDA UDI
FDA Product Code
JSM FDA UDI
GMDN Term
General specimen container IVD, additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2390 FDA UDI
Commercial Distribution
Not 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

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

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI

BD™ Universal Viral Transport for Viral, Specimens by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 27841176-c762-4c2e-829f-187739d3b96f 38 fields · synced May 30, 2026