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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 22, 2026

AV/215

426015772AVBLOODLINEEOWJ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Allmed Medical GmbH
UDI-DI code: 04260157727915
Reference / catalog number: AV/215

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View device family (Basic UDI)

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.

CW999
Contraindication: Patients with sensitivity to ETO should not be exposed to Allmed Arterial Venous Bloodlines.

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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: 04260157727915
Basic UDI-DI: 426015772AVBLOODLINEEOWJ
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. 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 HD
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)04260157727915

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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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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.