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Cascade

EUDAMED

Class III (EU MDR)

Ref FG0005

by Perflow Medical Ltd.

Identity

Trade Name
Cascade EUDAMED
Cascade L EUDAMED
Device Name
Cascade L EUDAMED
Cascade M EUDAMED
Model / Reference
FG0005 EUDAMED

Identifiers

Primary DI / UDI-DI
07290016441055 EUDAMED
Basic UDI-DI
B-07290016441055 EUDAMED
7290016441002W5 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 by Perflow Medical Ltd. — Class III — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

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

Sources (2)

  • EUDAMED d0e2e0f8-3ab3-4de5-a3cc-40c3cd2940e3 61 fields · synced Jun 17, 2026
  • EUDAMED 6d0362a5-c23e-49e7-8ba5-4c5aae3e63b7 61 fields · synced May 16, 2026