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Guiding rod , conical

EUDAMED

Class I (EU MDR)

Ref GRD226320B.

by Joimax GmbH

Identity

Trade Name
Guiding rod , conical EUDAMED
Device Name
Guiding Tube, Rod EUDAMED
Model / Reference
GRD226320B. EUDAMED

Identifiers

Primary DI / UDI-DI
04250337119586 EUDAMED
Basic UDI-DI
42503371DILADIL9L EUDAMED
Direct Marketing DI
04250337119586 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 rod , conical 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

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Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (1)

  • EUDAMED f688926c-0f2d-4b6a-9fba-28e3150676f8 61 fields · synced Jun 18, 2026