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Pubic Ramus Retractor

EUDAMED

Class I (EU MDR)

Ref 4050-0222

by Enztec Limited

Identity

Trade Name
Pubic Ramus Retractor EUDAMED
Device Name
Retractors and Frames EUDAMED
Model / Reference
4050-0222 EUDAMED

Identifiers

Primary DI / UDI-DI
09421028117555 EUDAMED
Basic UDI-DI
942102811GMN003124 EUDAMED
Direct Marketing DI
09421028117555 EUDAMED
EMDN Code
L0915 SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Pubic Ramus Retractor by Enztec Limited — 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
Enztec Limited
EUDAMED SRN
NZ-MF-000002264
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 8327a138-3d0a-45b8-adf5-ac781968d5f4 61 fields · synced Jul 8, 2026