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Rasps

EUDAMED

Class I (EU MDR)

Ref 58050018

by Hilbro Instruments (pvt) Ltd

Identity

Device Name
Rasps EUDAMED
Model / Reference
58050018 EUDAMED

Identifiers

Primary DI / UDI-DI
G11328050018 EUDAMED
Basic UDI-DI
++G11328050018CN EUDAMED
EMDN Code
L091201 ORTHOPAEDIC SURGERY RASPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Rasps by Hilbro Instruments (pvt) 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
PK-MF-000023402
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 25f370d2-c04b-4971-870b-7f82480d286f 61 fields · synced Jul 25, 2026