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C1 Cap / Roller set

EUDAMED

Class IIb (EU MDR)

Ref LaseMD Ultra

by Lutronic Corporation

Identity

Trade Name
C1 Cap / Roller set EUDAMED
Device Name
Thulium laser EUDAMED
Model / Reference
LaseMD Ultra EUDAMED

Identifiers

Primary DI / UDI-DI
08809447656274 EUDAMED
Basic UDI-DI
88094476511202AVS EUDAMED
EMDN Code
Z12011099 LASER SURGERY INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

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

C1 Cap / Roller set by Lutronic Corporation — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Unknown

CE/MDR

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Manufacturer

EUDAMED SRN
KR-MF-000009035
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED a65882d7-5019-4f01-b6ee-8381209d5a31 61 fields · synced Jul 9, 2026