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Twister

EUDAMED

Class IIa (EU MDR)

Ref 501200600

by Ceram Optec SIA

Identity

Device Name
Twister EUDAMED
Model / Reference
501200600 EUDAMED

Identifiers

Primary DI / UDI-DI
04049089005663 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

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

Sources (1)

  • EUDAMED 48fea713-cd29-4682-a5ae-5f96e29a30eb 61 fields · synced Jul 22, 2026