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VALIDATE® VITAMIN D Test Set

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 506ab

by LGC Clinical Diagnostics, Inc.

Identity

Trade Name
VALIDATE® VITAMIN D Test Set EUDAMED
Validate FDA UDI
Generic Name
Multiple form 25-hydroxy Vitamin D IVD, control FDA UDI
Device Name
VALIDATE® VITAMIN D Test Set EUDAMED
Validate Vit D is intended for the quantitative determination of Calibration Verification/Linearity on automated instruments. FDA UDI
Model / Reference
506ab EUDAMEDFDA UDI
Description
Validate Vit D is intended for the quantitative determination of Calibration Verification/Linearity on automated instruments. FDA UDI

Identifiers

Catalog Number
506ab FDA UDI
Primary DI / UDI-DI
00859110005845 EUDAMEDFDA UDI
Basic UDI-DI
B-00859110005845 EUDAMED
FDA Product Code
JJX FDA UDI
EMDN Code
W0102152006 ANAEMIA RELATED/VITAMIN CONTROLS EUDAMED
GMDN Term
Multiple form 25-hydroxy Vitamin D IVD, control FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Market of Registration
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

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

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

VALIDATE® VITAMIN D Test Set by LGC Clinical Diagnostics, Inc. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000029697
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED c161ede1-558e-4d14-a7d8-6c4556a0cec2 61 fields · synced Jul 22, 2026
  • FDA UDI 83c0a69e-6f1a-43e9-9a34-454dfa8ce12f 37 fields · synced May 30, 2026