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ReGrasp Clinician Pro 2

EUDAMED

Class I (EU MDR)

Ref EPKV2-EUModel EPKV2

by Rehabtronics

Identity

Trade Name
ReGrasp Clinician Pro 2 EUDAMED
Device Name
Electronic Positioning Kit Version 2 EUDAMED
Model / Reference
EPKV2 EUDAMED
EPKV2-EU EUDAMED

Identifiers

Primary DI / UDI-DI
17540176060014 EUDAMED
Basic UDI-DI
17540176060007K4 EUDAMED
EMDN Code
Z12062880,Z12062882,Z12062885,Z12062892,Z12062899 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

ReGrasp Clinician Pro 2 by Rehabtronics — 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
Rehabtronics
EUDAMED SRN
CA-MF-000018807
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED dce26d31-8372-4b73-80b1-169ac96acf41 61 fields · synced Jun 18, 2026