Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Klasse IIa Instrumente, chirurgisch… — 6 UDI-DI variants, MDR

MD Atlas
ARTIQO GmbH

Data from EUDAMED, last updated May 23, 2026

Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; maschinell angetriebene Instrumente, Bohrer

42511434022001C5

6 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: ARTIQO GmbH

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 42511434022001C5
Device name: Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; maschinell angetriebene Instrumente, Bohrer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: ARTIQO GmbH
SRN: DE-MF-000007336
Country: Germany
Email: info@artiqo.de
Phone: +49 2591-8931500

Variants by status

UDI-DI variants

6 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KRGD59CH6ST3N5HFYRXTJXT1

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

4-motion® Drillpin 3,204251143403173
4-motion® Drillpin 3,2 with head04251143403180
4-motion® Femoral Drill 6,404251143403234
4-motion® Femurbohrer Ø804251143408567
4-motion® Tibial Drill04251143403241
4-motion® Tibial Drill PSA04251143405924