Peripheral Angiographic Catheter

Trade name

Peripheral Angiographic Catheter

UDI-DI code

06938820561453

Basic UDI-DI

69388205000000000000003ZQ

Reference / catalog number

42.08.21452

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

• C0104020101PANORAMIC AND SELECTIVE PERIPHERAL DIAGNOSTIC ANGIOGRAPHY CATHETERS AND MICROCATHETERS

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

• CW009

  For single-patient use only. Do not reuse, reprocess, or resterilize this product. Reuse, reprocessing, or resterilization may compromise the structural integrity of the device and/or create a risk of contamination of the device, which could result in patient injury, illness, or death. Cleaning, disinfection, and resterilization may compromise the essential material and design characteristics of the device leading to device failure. • Do not use if package is opened or damaged.

No certificate specifically references this device's Basic UDI-DI.