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Armada™ 14 NC PTA Catheter

EUDAMED

Class IIa (EU MDR)

Ref 2300500-080

by Abbott Medical

Identity

Trade Name
Armada™ 14 NC PTA Catheter EUDAMED
Device Name
Peripheral Dilatation Catheter, Armada 14 NC EUDAMED
Model / Reference
2300500-080 EUDAMED

Identifiers

Primary DI / UDI-DI
08717648355639 EUDAMED
Basic UDI-DI
8717648PDC0006U5 EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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

Armada™ 14 NC PTA Catheter by Abbott Medical — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Abbott Medical
EUDAMED SRN
US-MF-000003851
Authorised Representative
Abbott Vascular International BE-AR-000002043

Sources (1)

  • EUDAMED cb24b16c-d590-43ff-8cd3-d7128abc3fbd 61 fields · synced Jul 9, 2026