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Proctology

EUDAMED

Class IIa (EU MDR)

Ref 501100250

by CeramOptec GmbH

Identity

Device Name
Proctology EUDAMED
Model / Reference
501100250 EUDAMED

Identifiers

Primary DI / UDI-DI
04049059516175 EUDAMED
Basic UDI-DI
404905910MZ EUDAMED
EMDN Code
Z12011085 LASER SURGERY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Category: Varicose vein lasing procedure kit

Proctology by CeramOptec GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Varicose vein lasing procedure kit.

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 34460326-58a2-4999-b876-ccab2997fada 61 fields · synced Jun 19, 2026