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VALIDATE® TDM1 Test Set

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 301ab

by LGC Clinical Diagnostics, Inc.

Identity

Trade Name
VALIDATE® TDM1 Test Set EUDAMED
Validate FDA UDI
Generic Name
Multiple therapeutic drugs/drugs of abuse IVD, control FDA UDI
Device Name
VALIDATE® TDM1 Test Set EUDAMED
Validate TDM1ab is intended for the quantitative determination of Calibration Verification/Linearity of drug analytes on automated instruments. FDA UDI
Model / Reference
301ab EUDAMEDFDA UDI
Description
Validate TDM1ab is intended for the quantitative determination of Calibration Verification/Linearity of drug analytes on automated instruments. FDA UDI

Identifiers

Catalog Number
301ab FDA UDI
Primary DI / UDI-DI
00859110005005 EUDAMEDFDA UDI
Basic UDI-DI
B-00859110005005 EUDAMED
FDA Product Code
DKB FDA UDI
EMDN Code
W0102152001 TDM/DRUG CONTROLS EUDAMED
GMDN Term
Multiple therapeutic drugs/drugs of abuse IVD, control FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
862.3200 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® TDM1 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

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Manufacturer

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

Sources (2)

  • EUDAMED 392ce8ed-4e8d-4327-9cf6-12d0dab35fa1 61 fields · synced Jul 9, 2026
  • FDA UDI 95afb3cb-4edc-4f94-86a7-f6ad98eb9bcb 37 fields · synced May 30, 2026