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Twister

EUDAMED

Class IIa (EU MDR)

Ref 501200200

by Ceram Optec SIA

Identity

Device Name
Twister EUDAMED
Model / Reference
501200200 EUDAMED

Identifiers

Primary DI / UDI-DI
04049089005359 EUDAMED
Basic UDI-DI
404908904NT EUDAMED
EMDN Code
Z12011085 LASER SURGERY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Latvia 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

Twister by Ceram Optec SIA — 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
Ceram Optec SIA
EUDAMED SRN
LV-MF-000021846

Sources (1)

  • EUDAMED 51db329c-804b-4cf2-8df7-df396c5195e9 61 fields · synced Jul 18, 2026