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LightTrail®

EUDAMED

Class IIa (EU MDR)

Ref M0068F64570

by Boston Scientific Corporation

Identity

Trade Name
LightTrail® EUDAMED
Device Name
LightTrail Reusable Laser Fibers EUDAMED
Model / Reference
M0068F64570 EUDAMED

Identifiers

Primary DI / UDI-DI
08714729939849 EUDAMED
Basic UDI-DI
01915060000000000000014MB EUDAMED
EMDN Code
Z12011085 LASER SURGERY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

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: Varicose vein lasing procedure kit

LightTrail® by Boston Scientific — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Varicose vein lasing procedure kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000004702
Authorised Representative
Boston Scientific Limited IE-AR-000003840

Sources (1)

  • EUDAMED f6349ce7-58c3-4453-8eb1-c97fa5edbd96 61 fields · synced Jun 18, 2026