Organization name

Alvimedica Tibbi Urunler San. ve Dis Tic. A.S.

SRN

TR-MF-000029915

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW010

  EUDAMED did not publish a description for this code.

Primary placement in Türkiye; available across 32 countries total.

Trade name

Alvision

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

08699195528431

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

086991955Alvision5D

Reference / catalog number

501110188630

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class III

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Alvision Interventional Cardiology Diagnostic Catheter SONES III 6F (SON 3 6F) 100cm - 10 Pack

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 6 MU170
• 100 MU10

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• C0104010101CARDIAC ANGIOGRAPHY DIAGNOSTIC CATHETERS

• Class III medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.