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Light Diagnostics ™ Poliovirus 1 Monoclonal Antibody

FDA UDI

Class I (US FDA UDI)

by Emd Millipore Corporation

Identity

Trade Name
Light Diagnostics ™ Poliovirus 1 Monoclonal Antibody FDA UDI
Generic Name
Poliovirus immunoglobulin M (IgM) antibody (serotypes PV1-PV3) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Poliovirus 1 Monoclonal Antibody FDA UDI
Model / Reference
3331 FDA UDI
Description
Poliovirus 1 Monoclonal Antibody FDA UDI

Identifiers

Catalog Number
3331 FDA UDI
Primary DI / UDI-DI
04053252369407 FDA UDI
510(k) Number
K940018 FDA UDI
FDA Product Code
GOE FDA UDI
GMDN Term
Poliovirus immunoglobulin M (IgM) antibody (serotypes PV1-PV3) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3405 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 ™ Poliovirus 1 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

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Manufacturer

Sources (1)

  • FDA UDI cac6a7f5-c465-4d7d-8eab-23ba3c16f4f3 38 fields · synced May 31, 2026