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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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Percutaneous Access Needle — 7 UDI-DI variants, MDR

MD Atlas
Wellgo Medical Products GmbH

Data from EUDAMED, last updated May 23, 2026

Percutaneous Access Needle

426064924PNSW

7 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: Wellgo Medical Products GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426064924PNSW
Device name: Percutaneous Access Needle
Device model: Percutaneous Access Needle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: Wellgo Medical Products GmbH
SRN: DE-MF-000033132
Country: Germany
Email: info@wellgomedical.com
Phone: +49 202 769162-10

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01JQ904XTKFBGAY0KZT712SB08

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

Percutaneous Access Needle04260649240045
Percutaneous Access Needle04260649240014
Percutaneous Access Needle04260649240076
Percutaneous Access Needle04260649240052
Percutaneous Access Needle04260649240038
Percutaneous Access Needle04260649240069
Percutaneous Access Needle04260649240021