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Snapshot 2026-10-22 · Link to EUDAMED

POWERFLEX™ PRO Percutaneous Transluminal Angioplasty (PTA) Catheter

UDI-DI 20705032059869Basic UDI-DI 07050320000000000000024CF

Class IIa · MDR · Cordis US Corp.

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
No
Measuring function
No
Reusable surgical
No
Certificates

No certificate found.

Snapshot 2026-10-22 · Link to EUDAMED

Manufacturer

Cordis US Corp.

SRN US-MF-000020031

US · Miami Lakes

manufacturer

Authorised representative: Cordis Cashel (IE-AR-000017793)

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Canonical device page: /device/powerflextm-pro-percutaneous-transluminal-angioplasty-pta-ca-9869 · UDI page: /udi/20705032059869

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