AV/215/1

Organization name

Allmed Medical GmbH

SRN

DE-MF-000007862

Manufacturer status

Active

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

• CW999

  Contraindication: Patients with sensitivity to ETO should not be exposed to Allmed Arterial Venous Bloodlines.

Primary placement in Slovenia; available across 1 country total.

Trade name

not provided

UDI-DI code

04260157727922

Basic UDI-DI

426015772AVBLOODLINEEOWJ

Reference / catalog number

AV/215/1

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

Arterial Venous Bloodline is intended to channel blood through external circuit for patients suffering from acute or chronic renal failure. The device is intended to be used for adult only, the device life time is 6 hours “maximum operating time”. Ethylene oxide (EO) sterilized, suitable for Nipro Surdial X HDF

Additional information URL

https://allmedgroup.com/e-ifu-repository/

Clinical sizes

No clinical sizes registered for this device.

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

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

• F020199ARTERIOVENOUS DIALYSIS LINES FOR HAEMODIALYSIS - HAEMOFILTRATION -HAEMODIAFILTRATION - OTHER