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Soundproof Booth

EUDAMED

Class I (EU MDR)

Ref S120+Model S80, S120, L150, L200, L250, L300, LS540, Z200, Z300, Z400, ZS540, ZS620, K100, K500, S100, S120+, L150+, L200+, L250+, L300+, Z200+, Z300+, A100, A300, A300+, Q220, Q220+, L280, Z280

by Beijing Joyo Sound Technology Co., Ltd.

Identity

Trade Name
Soundproof Booth EUDAMED
Device Name
Soundproof Booth EUDAMED
Model / Reference
S80, S120, L150, L200, L250, L300, LS540, Z200, Z300, Z400, ZS540, ZS620, K100, K500, S100, S120+, L150+, L200+, L250+, L300+, Z200+, Z300+, A100, A300, A300+, Q220, Q220+, L280, Z280 EUDAMED
S120+ EUDAMED

Identifiers

Primary DI / UDI-DI
06978272600164 EUDAMED
Basic UDI-DI
697827260SPB001QH EUDAMED
Direct Marketing DI
06978272600164 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER 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

Category: Device sterilization/disinfection container, reusable

Soundproof Booth by Beijing Joyo Sound Technology 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-000046128
Authorised Representative
BioDomi GmbH DE-AR-000016611

Sources (1)

  • EUDAMED 3b805cd0-717e-4e66-ba5e-6e22cc9bcf0a 61 fields · synced Jun 17, 2026