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Lift Arm

EUDAMED

Class I (EU MDR)

Ref KR8600-01

by Kinova

Identity

Trade Name
Lift Arm EUDAMED
Device Name
Jaco® EUDAMED
Model / Reference
KR8600-01 EUDAMED

Identifiers

Primary DI / UDI-DI
62867894100038 EUDAMED
Basic UDI-DI
628678941PJ00900006B5 EUDAMED
EMDN Code
Y242199 DEVICES FOR REACHING AND GRASPING OBJECTS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Lift Arm by Kinova — 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
Kinova
EUDAMED SRN
CA-MF-000003231
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (1)

  • EUDAMED ef0366cf-8065-41f8-98a0-36778d979d8f 61 fields · synced Jun 18, 2026