← Back to catalogue

Dpl

EUDAMED

Class IIa (EU MDR)

Ref DPL

by Australian Aesthetic Devices

Identity

Trade Name
DPL EUDAMED
Device Name
Multimodality Skin Treatment System EUDAMED
Model / Reference
DPL EUDAMED

Identifiers

Primary DI / UDI-DI
09362129000011 EUDAMED
Basic UDI-DI
93621290DPLIPLMS EUDAMED
Direct Marketing DI
09362129000011 EUDAMED
EMDN Code
X0502 HIGH INTENSITY ELECTROMAGNETIC RADIATION EMITTING EQUIPMENT WITHOUT AN INTENDED MEDICAL PURPOSE INTENDED FOR USE ON THE HUMAN BODY, FOR SKIN RESURFACING, TATTOO OR HAIR REMOVAL OR OTHER SKIN TREATMENT – INTENSE PULSED LIGHT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

Dpl by Australian Aesthetic Devices — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
AU-MF-000041530
Authorised Representative
Kingsmead Service B.V. NL-AR-000002066

Sources (1)

  • EUDAMED d99d0ae8-92ab-4568-8271-55bdd192ac4e 61 fields · synced Jun 19, 2026