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.

Mechanical articulated arm — 11 UDI-DI variants, MDR (KOELIS)

MD Atlas
KOELIS

Data from EUDAMED, last updated May 19, 2026

Mechanical articulated arm

3665134SteadyPro_01S6

11 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: KOELIS

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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3665134SteadyPro_01S6
Device name: Mechanical articulated arm
Device model: Steady Pro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 27, 2022

Manufacturer & authorised representative

Manufacturer

Name: KOELIS
SRN: FR-MF-000000830
Country: France
Email: info@koelis.com

Variants by status

UDI-DI variants

11 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

basicUdiUlid01GDX4SY2BHZAAMRDRDGB528W2

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

KSP.ARM03665134000738
Steady Pro Arm system03665134000738
KPHA.0003665134000592
KPHA.01.EC03665134000417
KPHA.01.EL03665134000448
KPHA.EC.203665134000424
KSP.SUPP.TR03665134000776
KSP.SUPP.TP03665134000745
KPHA.EL.203665134000493
KSP.SUPP.TP203665134000912
KSP.UNIVCLAMP03665134000806