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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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Reusable Biopsy Instrument — 2 UDI-DI variants, MDR

MD Atlas
Wellgo Medical Products GmbH

Data from EUDAMED, last updated May 23, 2026

Reusable Biopsy Instrument

426064924RBIHH

2 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

Reusable

Identity & classification

Basic UDI-DI: 426064924RBIHH
Device name: Reusable Biopsy Instrument
Device model: Reusable Biopsy Instrument
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 2, 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

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQTTVH2HK7KHN6BFG6SNWD3Z

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

W-Core II Reusable Biopsy Instrument04260649240922
W-Core Reusable Biopsy Instrument04260649240915