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Bio-Rad Platelia

FDA UDI

Class I (US FDA UDI)

by Clark Laboratories, Inc.

Identity

Trade Name
Bio-Rad Platelia FDA UDI
Generic Name
Epstein-Barr virus (EBV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
EBV-VCA IgG FDA UDI
Model / Reference
72937 FDA UDI
Description
EBV-VCA IgG FDA UDI

Identifiers

Catalog Number
72937 FDA UDI
Primary DI / UDI-DI
05391516746557 FDA UDI
510(k) Number
K883670 FDA UDI
FDA Product Code
GNP FDA UDI
GMDN Term
Epstein-Barr virus (EBV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3235 FDA UDI
Commercial Distribution
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

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

Category: Epstein-Barr virus (EBV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Bio-Rad Platelia by Clark Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Epstein-Barr virus (EBV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).

Cleared under the same submission

K883670 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5fc6cbdd-cbee-4137-bb8a-85fdbdb31d87 38 fields · synced Jun 8, 2026