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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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coflex-F™ Screwdriver — 2 UDI-DI variants, MDR (Paradigm Spine GmbH)

MD Atlas
Paradigm Spine GmbH

Data from EUDAMED, last updated May 23, 2026

coflex-F™ Screwdriver

0426014889002-008WV

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Paradigm Spine GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 0426014889002-008WV
Device name: coflex-F™ Screwdriver
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: Paradigm Spine GmbH
SRN: DE-MF-000011231
Country: Germany
Email: franz.menean@medagent.de
Phone: +49746399540

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KHKFE0JTYN0H71YMT8YF4JCR

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

RAT2020404260148890376
RAT2025404260148897672