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Sonic Muffs

EUDAMED

Class I (EU MDR)

Ref SM-001Model Sonic Muffs

by Conlett Technology Inc

Identity

Trade Name
Sonic Muffs EUDAMED
Device Name
Sonic Muffs EUDAMED
Model / Reference
Sonic Muffs EUDAMED
SM-001 EUDAMED

Identifiers

Primary DI / UDI-DI
06973596010385 EUDAMED
Basic UDI-DI
697359601SonicMuffsKH EUDAMED
Direct Marketing DI
06973596010385 EUDAMED
EMDN Code
T0399 PROTECTION DEVICES (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT PPE) - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Sonic Muffs by Conlett Technology Inc — 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-000002101
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 2248d584-60d3-472c-9229-7c5ddbde6b9c 61 fields · synced Jul 29, 2026