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Spectacle frame

EUDAMED

Class I (EU MDR)

Ref 06975289090018Model LT-500

by Shanghai Lthree Optical Co., Ltd.

Identity

Device Name
Spectacle frame EUDAMED
Model / Reference
LT-500 EUDAMED
06975289090018 EUDAMED

Identifiers

Primary DI / UDI-DI
06975289090018 EUDAMED
Basic UDI-DI
6975289090018F6 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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: Device sterilization/disinfection container, reusable

Spectacle frame by Shanghai Lthree Optical Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000040927
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED 5979bd61-0e46-40cf-a705-33c4cc25aa2f 61 fields · synced Jul 20, 2026