Identity
- Trade Name
- Genexus™ Dx Bottle 2 EUDAMED
- Device Name
- Ion Torrent™ Genexus™ Dx Sequencing Kit, a part of Ion Genexus™ Dx Reagents and Consumables EUDAMED
- Model / Reference
- A50866 (A50432) EUDAMED
Identifiers
- Primary DI / UDI-DI
- 10190302017534 EUDAMED
- Basic UDI-DI
- 0190302A50432RC EUDAMED
- EMDN Code
- W010699 GENETIC TESTS - OTHER EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
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
Genexus™ Dx Bottle 2 by Life Technologies Limited — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 0190302A50432RC | Class A | 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 a817ec05-7360-46bb-a4a0-2fd1cb9a089f 61 fields · synced Jul 10, 2026