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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/213+B — Class IIa MDR by Allmed Medical GmbH

MD Atlas
Allmed Medical GmbH

EUDAMED last updated this device on May 24, 2026

AV/213+B

426015772AVBLOODLINERQT

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Allmed Medical GmbH
UDI-DI code: 04260157725966
Reference / catalog number: AV/213+B

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View device family (Basic UDI)

Manufacturer information

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

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Allmed SafeFlow426015772SAFEFLOWR8UOn the market Allmed SafeFlow426015772SAFEFLOWR8UOn the market Allmed SafeFlow426015772SAFEFLOWEOXQOn the market Allmed SafeFlow426015772SAFEFLOWEOXQOn the market AV/197+B (H)426015772AVBLOODLINEEOWJOn the market

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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jun 1, 2016	Nov 3, 2023

Device identification

Trade name: not provided
UDI-DI code: 04260157725966
Basic UDI-DI: 426015772AVBLOODLINERQT
Reference / catalog number: AV/213+B
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. The device is intended to be used for adult only, the device life time is 6 hours “maximum operating time”. Gamma sterilized, suitable for Fresenius 2008/ 4008
Additional information URL: https://allmedgroup.com/e-ifu-repository/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04260157725966

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

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

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