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Monolisa™

FDA UDI

Class II (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
MONOLISA™ FDA UDI
Generic Name
Hepatitis B virus core immunoglobulin G (IgG) antibody IVD, control FDA UDI
Device Name
Anti-HBc IgM EIA, Cutoff Calibrator, 1.5 mL FDA UDI
Model / Reference
26203 FDA UDI
Description
Anti-HBc IgM EIA, Cutoff Calibrator, 1.5 mL FDA UDI

Identifiers

Catalog Number
26203 FDA UDI
Primary DI / UDI-DI
00847865013178 FDA UDI
PMA Number
P060034 FDA UDI
FDA Product Code
LOM FDA UDI
GMDN Term
Hepatitis B virus core immunoglobulin G (IgG) antibody IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3172 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 1.5 Milliliter FDA UDI

Category: Hepatitis B virus core immunoglobulin G (IgG) antibody IVD, control

Monolisa™ by Bio-Rad Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3daaa86e-b262-4e2c-8047-7a0e3dc00927 38 fields · synced May 30, 2026