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.

LENTULO — 45 UDI-DI variants, MDR (FKG Dentaire Sàrl)

MD Atlas
FKG Dentaire Sàrl

Data from EUDAMED, last updated May 23, 2026

LENTULO

764014241080100B3

45 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

Reusable

Identity & classification

Basic UDI-DI: 764014241080100B3
Device name: LENTULO
Device model: 02.171.25.030.GM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 26, 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

45 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

basicUdiUlid01KFXD430YH19YNS140XK40P2M

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

02.180.29.025.GS07640142420743
02.180.29.040.GS07640142420774
02.180.29.S25.GS07640142420781
02.180.21.S25.GS07640142420675
02.180.21.025.GS07640142420620
02.190.25.040.GM07640142420958
02.190.29.035.GM07640142421016
02.190.25.025.GM07640142420897
02.190.25.030.GM07640142420910
02.190.21.040.GM07640142420859
02.190.29.025.GM07640142420996
02.190.21.S25.GM07640142420873
02.190.21.030.GM07640142420828
02.190.29.S25.GM07640142421030
02.190.25.035.GM07640142420934
02.190.25.S25.GM07640142420989
02.190.21.025.GM07640142420804
02.190.29.030.GM07640142421009
02.190.29.040.GM07640142421023
02.190.21.035.GM07640142420842

1 2