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Sure-Vue

FDA UDI

Class II (US FDA UDI)

by Fisher Scientific Company L.l.c.

Identity

Trade Name
Sure-Vue FDA UDI
Generic Name
Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Sure-Vue Signature Mononucleosis FDA UDI
Model / Reference
23-200-275 FDA UDI
Description
Sure-Vue Signature Mononucleosis FDA UDI

Identifiers

Catalog Number
23200275 FDA UDI
Primary DI / UDI-DI
00613647000281 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

No

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

Yes

FDA UDI

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

Sure-Vue by Fisher Scientific Company L.l.c. — 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 0796dfec-40b4-4708-831b-f0f4eaaea7a1 35 fields · synced Jun 1, 2026