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Rotator Cuff Resection Guide

EUDAMED

Class I (EU MDR)

Ref 860-11-01

by JRI Orthopaedics Ltd

Identity

Trade Name
Rotator Cuff Resection Guide EUDAMED
Device Name
Guides EUDAMED
Model / Reference
860-11-01 EUDAMED

Identifiers

Primary DI / UDI-DI
05032982033481 EUDAMED
Basic UDI-DI
5032982/INSGUIDE22/MU EUDAMED
EMDN Code
L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Norway EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

Rotator Cuff Resection Guide by JRI Orthopaedics Ltd — 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

EUDAMED SRN
GB-MF-000007529
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 6191cc2b-294b-479e-95c7-19c8d1f19fc0 61 fields · synced Jul 16, 2026