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Kerrison 5x5

EUDAMED

Class I (EU MDR)

Ref 100-264

by AR Instrumed

Identity

Trade Name
Kerrison 5x5 EUDAMED
Device Name
Bone Rongeurs EUDAMED
Model / Reference
100-264 EUDAMED

Identifiers

Primary DI / UDI-DI
42518911109034 EUDAMED
Basic UDI-DI
4251891BONERONGEURSRN EUDAMED
Direct Marketing DI
42518911109034 EUDAMED
EMDN Code
L150302 DENTAL RONGEURS, 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

Kerrison 5x5 by AR Instrumed — 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
AR Instrumed
EUDAMED SRN
PK-MF-000019554
Authorised Representative
AR Instrumed Deutschland GmbH DE-AR-000014821

Sources (1)

  • EUDAMED 18ec7112-a6eb-4ff5-9c8f-8957eee5562e 61 fields · synced Jun 17, 2026