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BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit FDA UDI
Generic Name
Influenza A/B virus antigen IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Kit Flu A+B 30 Test Hospital Veritor FDA UDI
Model / Reference
256041 FDA UDI
Description
Kit Flu A+B 30 Test Hospital Veritor FDA UDI

Identifiers

Catalog Number
256041 FDA UDI
Primary DI / UDI-DI
00382902560418 FDA UDI
510(k) Number
K120049 FDA UDI
K121797 FDA UDI
K132256 FDA UDI
K132693 FDA UDI
K133138 FDA UDI
K151301 FDA UDI
K152874 FDA UDI
K160164 FDA UDI
FDA Product Code
PSZ FDA UDI
GMDN Term
Influenza A/B virus antigen IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3328 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

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: Influenza A/B virus antigen IVD, kit, rapid ICT, clinical

BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Influenza A/B virus antigen IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 394f0e76-574e-4a22-80e1-4c019a6d09ab 37 fields · synced May 30, 2026