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Neuro Duoflex 22cm
EUDAMEDClass I (EU MDR)
Ref 01-125-22Model 01-100-15 to 01-150-23
Identity
- Trade Name
- Neuro Duoflex 22cm EUDAMED
- Device Name
- ENT Diagnostic Instruments EUDAMED
- Model / Reference
- 01-100-15 to 01-150-23 EUDAMED01-125-22 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +G16401125220 EUDAMED
- Basic UDI-DI
- ++G1640110015to011M2 EUDAMED
- EMDN Code
- L1699 DIAGNOSTIC INSTRUMENTS, REUSABLE- OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Neuro Duoflex 22cm by Eltek Instruments Pvt Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++G1640110015to011M2 | Class I | Active |
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Manufacturer
- Manufacturer
- Eltek Instruments Pvt Ltd
- EUDAMED SRN
- PK-MF-000024315
- Authorised Representative
- CS Active LV-AR-000011602
Sources (1)
- EUDAMED 8814dfc7-5084-42db-8f5b-e6d17ad20304 61 fields · synced Jul 13, 2026