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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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Screw Drivers — 9 UDI-DI variants, MDR (devemed GmbH)

MD Atlas
devemed GmbH

Data from EUDAMED, last updated May 23, 2026

Screw Drivers

4061644PG1503013M

9 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: devemed GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4061644PG1503013M
Device name: Screw Drivers
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: devemed GmbH
SRN: DE-MF-000005568
Country: Germany
Email: info@devemed.de
Phone: +49 7467 9491990

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KH36V9CJ94907HVMA4Y1RSK1

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

4210-2104061644030507
4213-2104061644032006
4311-0004061644032891
4210-2004061644030491
4213-3104061644068463
4213-3004061644068449
4210-3004061644068401
4210-3104061644068425
4213-2004061644031528