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i-PAD

EUDAMED

Class IIb (EU MDR)

Ref CSO-I-004-R1Model CU-SPR

by CU Medical Systems, Inc.

Identity

Trade Name
i-PAD EUDAMED
Device Name
Defibrillator EUDAMED
Model / Reference
CU-SPR EUDAMED
CSO-I-004-R1 EUDAMED

Identifiers

Primary DI / UDI-DI
08809435481161 EUDAMED
Basic UDI-DI
B-08809435481161 EUDAMED
EMDN Code
Z12030501 SEMI-AUTOMATIC DEFIBRILLATORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

i-PAD by CU Medical Systems, Inc. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
KR-MF-000018333
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 4bc3116d-d609-4d1c-8dc7-eaa87c4a2218 61 fields · synced May 29, 2026