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Light Diagnostics ™ Adenovirus Monoclonal Antibody

FDA UDI

Class I (US FDA UDI)

by Emd Millipore Corporation

Identity

Trade Name
Light Diagnostics ™ Adenovirus Monoclonal Antibody FDA UDI
Generic Name
Multiple-genus respiratory virus antigen IVD, kit, fluorescent immunoassay FDA UDI
Device Name
Adenovirus Monoclonal Antibody FDA UDI
Model / Reference
5000 FDA UDI
Description
Adenovirus Monoclonal Antibody FDA UDI

Identifiers

Catalog Number
5000 FDA UDI
Primary DI / UDI-DI
04053252373411 FDA UDI
FDA Product Code
GNY FDA UDI
GMDN Term
Multiple-genus respiratory virus antigen IVD, kit, fluorescent immunoassay FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3020 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

Yes

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 ™ Adenovirus 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 0cdd3e2e-8d9a-4367-a33d-2771a05f2141 37 fields · synced Jun 6, 2026