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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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Scredriver blade — 7 UDI-DI variants, MDR

MD Atlas
Meditec Source GmbH & Co. KG

Data from EUDAMED, last updated Jun 2, 2026

Scredriver blade

426246385PG209K

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: Meditec Source GmbH & Co. KG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 426246385PG209K
Device name: Scredriver blade
Device model: Screwdriver
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 31, 2026

Manufacturer & authorised representative

Manufacturer

Name: Meditec Source GmbH & Co. KG
SRN: DE-MF-000006490
Country: Germany
Email: martin.streng@meditec-source.com
Phone: 017610429389

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KSZ700RZ4VA6EV40XPC6K3FF

Format

Summary

30 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
Market country
Issuing entity
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

2001-10104262463851391
2001-11104262463851414
2001-11204262463851421
2001-10204262463851407
2001-13104262463851445
2001-13104262463851438
2001-20104262463851469