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TECHNOLAS TENEO 317 Model2 V1

EUDAMED

Class IIb (EU MDR)

Ref 70010010TPV

by Technolas Perfect Vision GmbH

Identity

Trade Name
TECHNOLAS TENEO 317 Model2 V1 EUDAMED
Device Name
TECHNOLAS TENEO 317 Model 2 EUDAMED
Model / Reference
70010010TPV EUDAMED

Identifiers

Primary DI / UDI-DI
04050555106241 EUDAMED
Basic UDI-DI
4050555B000193 EUDAMED
EMDN Code
Z12011001 EXCIMER SURGICAL LASER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany 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

TECHNOLAS TENEO 317 Model2 V1 by Technolas Perfect Vision GmbH — 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
DE-MF-000007094

Sources (1)

  • EUDAMED bff935e8-7286-4025-9029-a5d5b8e03ce4 61 fields · synced Jun 19, 2026