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… — 51 UDI-DI variants, MDR

MD Atlas
ARTIQO GmbH

Data from EUDAMED, last updated May 23, 2026

Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; Probeimplantate

42511434022002C7

51 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: 42511434022002C7
Device name: Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; Probeimplantate
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 15, 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

51 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

basicUdiUlid01KRNTZPXH4NX1WYQ6Y3YGNSXZ

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® Femoral Trial left 2s04251143403258
4-motion® Femoral Trial left 3s04251143403265
4-motion® Femoral Trial left 4s04251143403272
4-motion® Femoral Trial left 5s04251143403289
4-motion® Femoral Trial left 5w04251143403302
4-motion® Femoral Trial left 6s04251143403296
4-motion® Femoral Trial left 6w04251143403319
4-motion® Femoral Trial left 7w04251143403326
4-motion® Femoral Trial left 8w04251143403333
4-motion® Femoral Trial left 9w04251143403340
4-motion® Femoral Trial right 2s04251143403357
4-motion® Femoral Trial right 3s04251143403364
4-motion® Femoral Trial right 4s04251143403371
4-motion® Femoral Trial right 5s04251143403388
4-motion® Femoral Trial right 5w04251143403401
4-motion® Femoral Trial right 6s04251143403395
4-motion® Femoral Trial right 6w04251143403418
4-motion® Femoral Trial right 7w04251143403425
4-motion® Femoral Trial right 8w04251143403432
4-motion® Femoral Trial right 9w04251143403449
4-motion® Tibial Base Plate PSA Sz. 104251143405771
4-motion® Tibial Base Plate PSA Sz. 1004251143405863
4-motion® Tibial Base Plate PSA Sz. 204251143405788
4-motion® Tibial Base Plate PSA Sz. 304251143405795
4-motion® Tibial Base Plate PSA Sz. 404251143405801

1 2 3