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Apolipoprotein Calibrator (apo Cal)

EUDAMEDFDA UDI

Class B (EU MDR)

Ref LP3023

by Randox Laboratories Limited

Identity

Trade Name
APOLIPOPROTEIN CALIBRATOR (APO CAL) EUDAMED
APO CAL FDA UDI
Generic Name
Multiple apolipoprotein IVD, calibrator FDA UDI
Device Name
APOLIPOPROTEIN CALIBRATOR EUDAMED
This product is intended for in-vitro use in the calibration of Apolipoprotein A-I and Apolipoprotein B assays. FDA UDI
Model / Reference
LP3023 EUDAMEDFDA UDI
Description
This product is intended for in-vitro use in the calibration of Apolipoprotein A-I and Apolipoprotein B assays. FDA UDI

Identifiers

Catalog Number
LP3023 FDA UDI
Primary DI / UDI-DI
05055273204414 EUDAMEDFDA UDI
Basic UDI-DI
50552732BAPOCAL01594 EUDAMED
510(k) Number
K023158 FDA UDI
FDA Product Code
JIX FDA UDI
EMDN Code
W0102152203 SPECIFIC PROTEIN STANDARDS AND CALIBRATORS EUDAMED
GMDN Term
Multiple apolipoprotein IVD, calibrator FDA UDI

Classification

Device Class
Class B EUDAMED
Class II FDA UDI
Regulation Number
862.1150 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

Yes

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Apolipoprotein Calibrator (apo Cal) by Randox Laboratories Limited — Class B — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
XI-MF-000028410

Sources (2)

  • EUDAMED 864a2019-737f-4dd6-a61e-fe6fc5c19884 61 fields · synced Jul 9, 2026
  • FDA UDI ee4364e1-bc7a-4609-93a0-28d8e7de0ea4 37 fields · synced May 30, 2026