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.

R-Motion — 220 UDI-DI variants, MDR (FKG Dentaire Sàrl)

MD Atlas
FKG Dentaire Sàrl

Data from EUDAMED, last updated May 23, 2026

R-Motion

7640142410401019R

220 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: FKG Dentaire Sàrl

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: 7640142410401019R
Device name: R-Motion
Device model: S1.7B0.00.0FI.FK
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: FKG Dentaire Sàrl
SRN: CH-MF-000017925
Country: Switzerland
Email: info@fkg.ch
Phone: +41329242244

Authorised representative

Name: Emergo Europe B.V.
SRN: NL-AR-000000116
Country: Netherlands
Phone: +31 70 345 8570

Variants by status

UDI-DI variants

220 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

basicUdiUlid01KF0C1Z12Y0HX97WSFHV11NA1

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

X7300425HTS07640142449393
X7170429HTS07640142449430
X7300621HTS07640142449539
X70621ASST07640142449744
X7350421HTS07640142449331
X7200421HTS07640142449300
X7450421HTS07640142449355
X7200425HTS07640142449379
X7400425HTS07640142449416
X7450425HTS07640142449423
X7300429HTS07640142449461
X7200629HTS07640142449652
X7300629HTS07640142449676
X7200429HTS07640142449447
X7400625HTS07640142449621
X7250629HTS07640142449669
X7350621HTS07640142449546
X7450625HTS07640142449638
X70421ASST07640142449713
X7400429HTS07640142449485
X7170629HTS07640142449645
X7250625HTS07640142449591
X7350629HTS07640142449683
X7400629HTS07640142449690
X7200625HTS07640142449584

5 6 7 8 9