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Light Diagnostics ™ Influenza A & B Control Slides

FDA UDI

Class I (US FDA UDI)

by Emd Millipore Corporation

Identity

Trade Name
Light Diagnostics ™ Influenza A & B Control Slides FDA UDI
Generic Name
Multiple-genus respiratory virus antigen IVD, kit, fluorescent immunoassay FDA UDI
Device Name
Influenza A & B Control Slides FDA UDI
Model / Reference
5010-5 FDA UDI
Description
Influenza A & B Control Slides FDA UDI

Identifiers

Catalog Number
5010-5 FDA UDI
Primary DI / UDI-DI
04053252373435 FDA UDI
FDA Product Code
GNW FDA UDI
GMDN Term
Multiple-genus respiratory virus antigen IVD, kit, fluorescent immunoassay FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3330 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 ™ Influenza A & B Control Slides 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 8c7f0665-3eb6-46a6-9de3-857bade857af 37 fields · synced May 30, 2026