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LaseMD Ultra

EUDAMED

Class IIb (EU MDR)

Ref LaseMD Ultra

by Cynosure Lutronic Technology Corporation

Identity

Trade Name
LaseMD Ultra EUDAMED
Device Name
Thulium Laser EUDAMED
Model / Reference
LaseMD Ultra EUDAMED

Identifiers

Primary DI / UDI-DI
08800291820590 EUDAMED
Basic UDI-DI
88002918211202AH9 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

LaseMD Ultra by Cynosure Lutronic Technology Corporation — Class IIb — 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

EUDAMED SRN
KR-MF-000047499
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 74688807-08ae-4969-ba74-08fd2751b3c3 61 fields · synced Jul 10, 2026