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HydroCheck-E

EUDAMED

Class I (EU MDR)

Ref 77080-06D

by Pereg GmbH

Identity

Trade Name
HydroCheck-E EUDAMED
Device Name
Indicator for validation of cleaning performance EUDAMED
Model / Reference
77080-06D EUDAMED

Identifiers

Primary DI / UDI-DI
14260052660932 EUDAMED
Basic UDI-DI
426005266ResidueDetectUU EUDAMED
EMDN Code
Z12029080 VARIOUS INSTRUMENTS FOR ENDOSCOPY AND MINI-INVASIVE SURGERY - HARDWARE ACCESSORIES 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

HydroCheck-E by Pereg GmbH — 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
Pereg GmbH
EUDAMED SRN
DE-MF-000048645

Sources (1)

  • EUDAMED c6af0465-bb72-4d9c-b058-8a7d3353d876 61 fields · synced Oct 6, 2026