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Ultrasonic Cavitation Performance Test Indicator

EUDAMED

Class I (EU MDR)

Ref MZS-5635 Dia 12mmx32mmModel MZS-5635

by Mediwish Co., Ltd

Identity

Device Name
ULTRASONIC CAVITATION PERFORMANCE TEST INDICATOR EUDAMED
Model / Reference
MZS-5635 EUDAMED
MZS-5635 Dia 12mmx32mm EUDAMED

Identifiers

Primary DI / UDI-DI
06974409693030 EUDAMED
Basic UDI-DI
697440969UCPTIVY EUDAMED
EMDN Code
S0199 DEVICES FOR STERILISATION AND PACKAGING (EXCLUDING CAT. D - Z) - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Ultrasonic Cavitation Performance Test Indicator by Mediwish 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

Manufacturer
Mediwish Co., Ltd
EUDAMED SRN
CN-MF-000008849
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED ccf8e4a1-b340-44f3-92dd-459de171339d 61 fields · synced Jul 11, 2026