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Glenoid Retractor - Forked

EUDAMED

Class I (EU MDR)

Ref 870-29-00

by JRI Orthopaedics Ltd

Identity

Trade Name
Glenoid Retractor - Forked EUDAMED
Device Name
Spreaders and Retractors for Orthopaedic Surgery EUDAMED
Model / Reference
870-29-00 EUDAMED

Identifiers

Primary DI / UDI-DI
05032982033962 EUDAMED
Basic UDI-DI
5032982/INSLRET15/Z9 EUDAMED
EMDN Code
L0915 SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, 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

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

Glenoid Retractor - Forked 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 5befc357-2efc-4c8b-bbeb-4f4e744a96cf 61 fields · synced Jul 14, 2026