← Back to catalogue
Oncomine™ Dx Express Test - Plasma - v2.1.0 ADF
EUDAMEDClass IVD General (EU MDR)
Ref A40010734
Identity
- Trade Name
- Oncomine™ Dx Express Test - Plasma - v2.1.0 ADF EUDAMED
- Device Name
- Oncomine™ Dx Express Test - Plasma - v2.1.0 ADF, a part of Ion Torrent™ Oncomine™ Dx Express Test EUDAMED
- Model / Reference
- A40010734 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-USMF000023929A40010738W EUDAMED
- Basic UDI-DI
- B-USMF000023929A40010738W EUDAMED
- EMDN Code
- W02050182 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - SOFTWARE ACCESSORIES EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
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
Oncomine™ Dx Express Test - Plasma - v2.1.0 ADF by Life Technologies Limited — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-USMF000023929A40010738W | Class IVD General | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Life Technologies Corporation
- EUDAMED SRN
- US-MF-000023929
- Authorised Representative
- Life Technologies Europe B.V. NL-AR-000021890
Sources (1)
- EUDAMED 02b5f1ca-9580-4bed-8f83-a2d58e0c23be 61 fields · synced Jun 19, 2026