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Bare Fiber

EUDAMED

Class IIa (EU MDR)

Ref 503200105

by CeramOptec GmbH

Identity

Device Name
Bare Fiber EUDAMED
Model / Reference
503200105 EUDAMED

Identifiers

Primary DI / UDI-DI
04049059519305 EUDAMED
Basic UDI-DI
404905902N2 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

Bare Fiber 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 5102bb2f-a61d-4c01-b1a6-24fe2a660127 61 fields · synced Jun 18, 2026