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HemoCheck-S

EUDAMED

Class I (EU MDR)

Ref 67067-12

by Pereg GmbH

Identity

Trade Name
HemoCheck-S EUDAMED
Device Name
Indicator for validation of cleaning performance EUDAMED
Model / Reference
67067-12 EUDAMED

Identifiers

Primary DI / UDI-DI
14260052660123 EUDAMED
Basic UDI-DI
426005266ResidueDetectUU EUDAMED
Direct Marketing DI
14260052660123 EUDAMED
EMDN Code
Z12019080 VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY 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

HemoCheck-S 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 f9d5bd69-746b-49fa-8074-35e9d2878260 61 fields · synced Oct 6, 2026