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VIROCLEAR MuMZ

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
VIROCLEAR MuMZ FDA UDI
Generic Name
Varicella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, control FDA UDI
Device Name
VIROCLEAR MuMZ (An unassayed (human) serology control.) FDA UDI
Model / Reference
00133 FDA UDI
Description
VIROCLEAR MuMZ (An unassayed (human) serology control.) FDA UDI

Identifiers

Catalog Number
00133 FDA UDI
Primary DI / UDI-DI
00847661002666 FDA UDI
FDA Product Code
OHQ FDA UDI
GMDN Term
Varicella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

No

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

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: Varicella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, controlMeasles virus immunoglobulin G (IgG) antibody IVD, controlMumps virus immunoglobulin G (IgG) antibody IVD, control

VIROCLEAR MuMZ by Bio-Rad Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Measles virus immunoglobulin G (IgG) antibody IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio-Rad Laboratories

Sources (1)

  • FDA UDI 8cfda2a6-ec04-4e3d-97ac-3ea50439a013 36 fields · synced May 30, 2026