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Kendou

EUDAMED

Class I (EU MDR)

Ref SYQ13808Model 15940, 2011, 8013, 2033, 237, 020, 9707, 228, 3181, 668, 5101, 1921, 2024, 2211, 1920, 1004, 8158, 908, 522, 128, 277, 1102, 818, 2243;

by Chongqing Shiyuanqing Technology Co., Ltd

Identity

Trade Name
KENDOU EUDAMED
Device Name
Reading Glasses EUDAMED
Model / Reference
15940, 2011, 8013, 2033, 237, 020, 9707, 228, 3181, 668, 5101, 1921, 2024, 2211, 1920, 1004, 8158, 908, 522, 128, 277, 1102, 818, 2243; EUDAMED
SYQ13808 EUDAMED

Identifiers

Primary DI / UDI-DI
06977374960015 EUDAMED
Basic UDI-DI
6977374960015GV EUDAMED
EMDN Code
Y210324 NEAR SIGHTEDNESS TELESCOPIC SYSTEMS/SPECTACLES EUDAMED

Classification

Device Class
Class I 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

Kendou by Chongqing Shiyuanqing Technology Co., Ltd — Class I — 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
CN-MF-000041637
Authorised Representative
Humiss Beratung GmbH DE-AR-000023447

Sources (1)

  • EUDAMED 3523903e-72da-4b9b-9217-1543f310c86a 61 fields · synced Jun 17, 2026