← Back to catalogue
VALIDATE® TDM1 Test Set
EUDAMEDFDA UDIClass IVD General (EU MDR)
Ref 301dbModel VALIDATE® TDM1 Test Set
Identity
- Trade Name
- VALIDATE® TDM1 Test Set EUDAMEDValidate FDA UDI
- Generic Name
- Multiple therapeutic drugs/drugs of abuse IVD, control FDA UDI
- Device Name
- VALIDATE® TDM1 Test Set EUDAMEDValidate TDM1db is intended for the quantitative determination of Calibration Verification/Linearity of drug analytes on automated instruments. FDA UDI
- Model / Reference
- VALIDATE® TDM1 Test Set EUDAMED301db EUDAMEDFDA UDI
- Description
- Validate TDM1db is intended for the quantitative determination of Calibration Verification/Linearity of drug analytes on automated instruments. FDA UDI
Identifiers
- Catalog Number
- 301db FDA UDI
- Primary DI / UDI-DI
- 00859110005036 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00859110005036 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 EUDAMEDClass 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-00859110005036 | Class IVD General | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD General | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- LGC Clinical Diagnostics, Inc.
- EUDAMED SRN
- US-MF-000029697
- Authorised Representative
- MediMark Europe Sarl. FR-AR-000000182
Sources (2)
- EUDAMED 39da5501-3f67-4bb4-801a-85a908b8dac9 61 fields · synced Jun 18, 2026
- FDA UDI f9371457-fbd2-4776-b694-5a824eb67626 37 fields · synced May 30, 2026