← Back to catalogue

Light Diagnostics ™ Coxsackievirus B5 Monoclonal Antibody

FDA UDI

Class I (US FDA UDI)

by Emd Millipore Corporation

Identity

Trade Name
Light Diagnostics ™ Coxsackievirus B5 Monoclonal Antibody FDA UDI
Generic Name
Coxsackie A/B virus antigen IVD, reagent FDA UDI
Device Name
Coxsackievirus B5 Monoclonal Antibody FDA UDI
Model / Reference
3308 FDA UDI
Description
Coxsackievirus B5 Monoclonal Antibody FDA UDI

Identifiers

Catalog Number
3308 FDA UDI
Primary DI / UDI-DI
04053252332371 FDA UDI
510(k) Number
K940472 FDA UDI
FDA Product Code
GNM FDA UDI
GMDN Term
Coxsackie A/B virus antigen IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3145 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Light Diagnostics ™ Coxsackievirus B5 Monoclonal Antibody by Emd Millipore Corporation — 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 cbe099d7-3fa7-45c5-a1ab-107d90bf0d87 38 fields · synced May 30, 2026