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Acceava® Mono Cassette

FDA UDI

Class II (US FDA UDI)

by Alere North America, Llc

Identity

Trade Name
Acceava® Mono Cassette FDA UDI
Generic Name
Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical FDA UDI
Model / Reference
92407 FDA UDI

Identifiers

Primary DI / UDI-DI
10859035006238 FDA UDI
FDA Product Code
KTN FDA UDI
GMDN Term
Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical

Acceava® Mono Cassette by Alere North America, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 81cbc70c-5244-4901-8050-0a08c89de51f 34 fields · synced May 31, 2026