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Cascade M

EUDAMED

Class III (EU MDR)

Ref FG0006

by Perflow Medical Ltd.

Identity

Trade Name
Cascade M EUDAMED
Cascade EUDAMED
Device Name
Cascade M EUDAMED
Model / Reference
FG0006 EUDAMED

Identifiers

Primary DI / UDI-DI
07290016441062 EUDAMED
Basic UDI-DI
7290016441002W5 EUDAMED
B-07290016441062 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 M 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 347f2df0-1b6e-4912-afbb-b2cc14c57aa2 61 fields · synced Jul 31, 2026
  • EUDAMED 893d233f-616c-453c-a967-7f89e8c8bdbb 61 fields · synced May 17, 2026