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Balloon Inflation Devices Kit

EUDAMED

Class I (EU MDR)

Ref BID817127Ref BID817128Ref BID817130

by SWL Medizin GmbH

Identity

Device Name
Balloon Inflation Devices Kit EUDAMED
Model / Reference
BID817127 EUDAMED
BID817128 EUDAMED
BID817130 EUDAMED

Identifiers

Primary DI / UDI-DI
04251790271279 EUDAMED
04251790271286 EUDAMED
04251790271309 EUDAMED
Basic UDI-DI
B-04251790271279 EUDAMED
B-04251790271286 EUDAMED
B-04251790271309 EUDAMED
EMDN Code
A02010401 SYRINGES FOR CONTRAST MEDIA INJECTOR, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

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

Category: Angiography kit

Balloon Inflation Devices Kit by SWL Medizin GmbH — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Angiography kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
SWL Medizin GmbH
EUDAMED SRN
DE-MF-000008000

Sources (3)

  • EUDAMED c2d6b308-cf33-4346-a501-9574180c2c0c 61 fields · synced Jul 20, 2026
  • EUDAMED 56e178ec-8266-4021-9be2-ca2d07514cee 61 fields · synced May 16, 2026
  • EUDAMED 595e7d4d-13f2-424d-a69d-35f610d73d7b 61 fields · synced May 17, 2026