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Guiding Tube, eccentrically cannulated, purple
EUDAMEDClass I (EU MDR)
Ref GRD177440
by Joimax GmbH
Identity
- Trade Name
- Guiding Tube, eccentrically cannulated, purple EUDAMED
- Device Name
- Guiding Tube, Rod EUDAMED
- Model / Reference
- GRD177440 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250337119197 EUDAMED
- Basic UDI-DI
- 42503371DILADIL9L EUDAMED
- Direct Marketing DI
- 04250337119197 EUDAMED
- EMDN Code
- L1199 NEUROSURGERY 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
Guiding Tube, eccentrically cannulated, purple by Joimax GmbH — 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 | 42503371DILADIL9L | Class I | Active |
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Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (1)
- EUDAMED ded7e23e-fed1-4a00-a23c-59b217409271 61 fields · synced Jul 21, 2026