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BD Veritor SARS-CoV-2 Control Swab Set

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Veritor SARS-CoV-2 Control Swab Set FDA UDI
Generic Name
SARS-CoV-1/SARS-CoV-2 antigen IVD, control FDA UDI
Device Name
Veritor COVID Gen 2 control swab set FDA UDI
Model / Reference
256138 FDA UDI
Description
Veritor COVID Gen 2 control swab set FDA UDI

Identifiers

Catalog Number
256138 FDA UDI
Primary DI / UDI-DI
00382902561385 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
SARS-CoV-1/SARS-CoV-2 antigen IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: SARS-CoV-1/SARS-CoV-2 antigen IVD, control

BD Veritor SARS-CoV-2 Control Swab Set 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

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Manufacturer

Sources (1)

  • FDA UDI ec0054d9-d52c-42c2-a20e-971d1ad864aa 36 fields · synced Jun 8, 2026