Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

AV/H951 — Class IIa MDR by Allmed Medical GmbH

MD Atlas
Allmed Medical GmbH

EUDAMED last updated this device on May 23, 2026

AV/H951

426015772AVBLOODLINEEOWJ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Allmed Medical GmbH
UDI-DI code: 04260157721876
Reference / catalog number: AV/H951

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in EL; available across 1 country total.

Country	On market since	Until
ELPrimary placement	Jul 29, 2016	Feb 17, 2021

Device identification

Trade name: not provided
UDI-DI code: 04260157721876
Basic UDI-DI: 426015772AVBLOODLINEEOWJ
Reference / catalog number: AV/H951
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 Fresenius Machine
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)04260157721876

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

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

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

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

Become a partner of MD Atlas

Related devices

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.