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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

AV/215 — Class IIa MDR by Allmed Medical GmbH

MD Atlas
Allmed Medical GmbH

EUDAMED last updated this device on May 14, 2024

AV/215

426015772AVBLOODLINERQT

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Allmed Medical GmbH
UDI-DI code: 04260157727779
Reference / catalog number: AV/215

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Manufacturer information

Organization name: Allmed Medical GmbH
SRN: DE-MF-000007862
Manufacturer status: Active

Critical warnings

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

CW010
Allmed recommends use of a dialysis machine that is equipped with a volumetric ultrafiltration unit, an accurate UF control system and a precise weight system for hemodiafiltration.

Market distribution

Primary placement in EL; available across 1 country total.

Country	On market since	Until
ELPrimary placement	May 4, 2021	May 14, 2024

Device identification

Trade name: not provided
UDI-DI code: 04260157727779
Basic UDI-DI: 426015772AVBLOODLINERQT
Reference / catalog number: AV/215
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

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
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

F020199ARTERIOVENOUS DIALYSIS LINES FOR HAEMODIALYSIS - HAEMOFILTRATION -HAEMODIAFILTRATION - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.