OSOM Ultra Flu Aspirate 25T Kit

FDA UDI

Class II (US FDA UDI)

by Sekisui Diagnostics, LLC

Identity

Trade Name: OSOM Ultra Flu Aspirate 25T Kit FDA UDI
Generic Name: Nasopharyngeal aspirate container IVD FDA UDI
Device Name: OSOM Ultra Flu Aspirate 25T Kit FDA UDI
Model / Reference: 1007 FDA UDI
Description: OSOM Ultra Flu Aspirate 25T Kit FDA UDI

Identifiers

Catalog Number: 1007 FDA UDI
Primary DI / UDI-DI: 00742860100239 FDA UDI
FDA Product Code: PSZ FDA UDI
GMDN Term: Nasopharyngeal aspirate container IVD FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 866.3328 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Nasopharyngeal aspirate container IVD

OSOM Ultra Flu Aspirate 25T Kit by Sekisui Diagnostics, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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BioSign Flu A+B Nasal Wash/Aspirate Kit — PRINCETON BIOMEDITECH CORP. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Sekisui Diagnostics, LLC

Sources (1)

FDA UDI 7b29495a-85cd-4cdd-9ede-f0df1133dd4a 35 fields · synced Jun 9, 2026