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Cascade 17

EUDAMED

Class III (EU MDR)

Ref FG0009

by Perflow Medical Ltd.

Identity

Trade Name
Cascade 17 EUDAMED
Cascade EUDAMED
Device Name
Cascade M EUDAMED
Cascade 17 EUDAMED
Model / Reference
FG0009 EUDAMED

Identifiers

Primary DI / UDI-DI
07290016441093 EUDAMED
Basic UDI-DI
7290016441002W5 EUDAMED
B-07290016441093 EUDAMED
EMDN Code
C99 CARDIOCIRCULATORY DEVICES - OTHER EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Cascade 17 by Perflow Medical Ltd. — Class III — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IL-MF-000009315
Authorised Representative
MedNet EC-REP III GmbH DE-AR-000011191

Sources (2)

  • EUDAMED d1d4fe56-7bf4-44e2-937e-4091fa749776 61 fields · synced Jun 20, 2026
  • EUDAMED 96bca5dd-cce0-4833-826b-ef81c6d0ac53 61 fields · synced May 18, 2026