← Back to catalogue

FlexCath Cross Transseptal Solution

EUDAMED

Class III (EU MDR)

Ref 900301

by Acutus Medical, Inc.

Identity

Trade Name
FlexCath Cross Transseptal Solution EUDAMED
Device Name
AcQCross Qx Integrated Transseptal Dilator/Needle EUDAMED
Model / Reference
900301 EUDAMED

Identifiers

Primary DI / UDI-DI
00850027837772 EUDAMED
Basic UDI-DI
0850027837ACQCROSSP3 EUDAMED
EMDN Code
C01020101 CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS 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

FlexCath Cross Transseptal Solution by Acutus Medical, Inc. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000019413
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED aa7e3a2f-68ac-48d6-a9af-37a73574ebd5 61 fields · synced May 22, 2026