← Back to catalogue

Guiding Tube, eccentrically cannulated, red

EUDAMED

Class I (EU MDR)

Ref GRD196440

by Joimax GmbH

Identity

Trade Name
Guiding Tube, eccentrically cannulated, red EUDAMED
Device Name
Guiding Tube, Rod EUDAMED
Model / Reference
GRD196440 EUDAMED

Identifiers

Primary DI / UDI-DI
04250337119180 EUDAMED
Basic UDI-DI
42503371DILADIL9L EUDAMED
Direct Marketing DI
04250337119180 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, red 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (1)

  • EUDAMED 5f37d1c0-4cb7-4ea0-a35f-4a9accebec8e 61 fields · synced Jun 19, 2026