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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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Arterial Venous Dialysis Fistula Needle — 5 UDI-DI variants, MDR

MD Atlas
Allmed Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Arterial Venous Dialysis Fistula Needle

426015772FNEEDLEEO2K

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Allmed Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426015772FNEEDLEEO2K
Device name: Arterial Venous Dialysis Fistula Needle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Allmed Medical GmbH
SRN: DE-MF-000007862
Country: Germany
Email: juergen.haaser@allmedgroup.com
Phone: + 49 151 5877 8237

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KRZZ1YXZ2X45SPA5F7MW34VF

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

FN17GVR/3004260157724778
FN16GVR/3004260157722200
AVFN16GR/1504260157724891
FN17GAR/3004260157722224
AVFN16GR/3004260157722248