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LASERNEEDLE Touch

EUDAMED

Class IIa (EU MDR)

Ref 13001Model LASERNEEDLE Touch Allround

by Laserneedle GmbH

Identity

Trade Name
LASERNEEDLE Touch EUDAMED
Device Name
LASERNEEDLE Touch Allround EUDAMED
Model / Reference
LASERNEEDLE Touch Allround EUDAMED
13001 EUDAMED

Identifiers

Primary DI / UDI-DI
04260649160060 EUDAMED
Basic UDI-DI
B-04260649160060 EUDAMED
EMDN Code
Z120615 THERAPEUTIC LASERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

LASERNEEDLE Touch by Laserneedle GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Manufacturer's product page: Laserneedle Touch Orthophys

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Laserneedle GmbH
EUDAMED SRN
DE-MF-000023539

Sources (1)

  • EUDAMED 06e36172-4bd4-4264-b923-047f5eebe42a 61 fields · synced May 22, 2026