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Mercury

EUDAMED

Class IIa (EU MDR)

Ref POTW831582

by SWL Medizin GmbH

Identity

Trade Name
Mercury EUDAMED
Device Name
PTA Balloon Dilatation Catheter EUDAMED
Model / Reference
POTW831582 EUDAMED

Identifiers

Primary DI / UDI-DI
04251790215822 EUDAMED
Basic UDI-DI
42517902POTWQW EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

Category: Peripheral angioplasty balloon catheter, basic

Mercury by SWL Medizin GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
SWL Medizin GmbH
EUDAMED SRN
DE-MF-000008000

Sources (1)

  • EUDAMED ab49f624-8c97-4a0e-bbc9-265ea9aa4700 61 fields · synced Jun 19, 2026