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Cascade

EUDAMED

Class III (EU MDR)

Ref FG0007

by Perflow Medical Ltd.

Identity

Trade Name
Cascade EUDAMED
Cascade L Agile EUDAMED
Device Name
Cascade L Agile EUDAMED
Cascade M EUDAMED
Model / Reference
FG0007 EUDAMED

Identifiers

Primary DI / UDI-DI
07290016441079 EUDAMED
Basic UDI-DI
B-07290016441079 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 — 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 952774e5-0fb3-4782-b51c-3956837341df 61 fields · synced Jul 12, 2026
  • EUDAMED 2872e6e3-1597-4bed-b945-5aa3f3c5c5ae 61 fields · synced May 17, 2026