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Healite Ii

EUDAMED

Class IIa (EU MDR)

Ref HEALITE II

by Cynosure Lutronic Technology Corporation

Identity

Trade Name
HEALITE II EUDAMED
Device Name
Phototherapy Unit EUDAMED
Model / Reference
HEALITE II EUDAMED

Identifiers

Primary DI / UDI-DI
08800291820330 EUDAMED
Basic UDI-DI
88002918210704AJ7 EUDAMED
EMDN Code
Z12040299 GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class IIa 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

Category: Dermatological laser beam guiding handpiece

Healite Ii by Cynosure Lutronic Technology Corporation — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological laser beam guiding handpiece.

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 6fa1224b-f79b-4965-8965-571272c836e8 61 fields · synced Jul 30, 2026