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Proctology

EUDAMED

Class IIa (EU MDR)

Ref 501805200

by CeramOptec GmbH

Identity

Device Name
Proctology EUDAMED
Model / Reference
501805200 EUDAMED

Identifiers

Primary DI / UDI-DI
04049059517448 EUDAMED
Basic UDI-DI
404905910MZ EUDAMED
EMDN Code
Z12011085 LASER SURGERY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Proctology by CeramOptec GmbH — Class IIa — 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
CeramOptec GmbH
EUDAMED SRN
DE-MF-000005607

Sources (1)

  • EUDAMED d464a33c-a0d8-4aae-9b92-944803e7b7b4 61 fields · synced Jun 18, 2026