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OSOM Influenza Control Kit

FDA UDI

Class I (US FDA UDI)

by Sekisui Diagnostics, LLC

Identity

Trade Name
OSOM Influenza Control Kit FDA UDI
Generic Name
Influenza A/B virus antigen IVD, control FDA UDI
Model / Reference
191 FDA UDI

Identifiers

Catalog Number
191 FDA UDI
Primary DI / UDI-DI
00742860100147 FDA UDI
FDA Product Code
GNX FDA UDI
GMDN Term
Influenza A/B virus antigen IVD, control 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

OSOM Influenza Control Kit by Sekisui Diagnostics, LLC — 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 5afe36c6-63ba-4960-a972-79eee079ea07 34 fields · synced Jun 9, 2026