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.

RISKONTROL tips — 13 UDI-DI variants, MDR (ACTEON MANUFACTURING)

MD Atlas
ACTEON MANUFACTURING

Data from EUDAMED, last updated May 19, 2026

RISKONTROL tips

376024300riskontrolSH

13 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: ACTEON MANUFACTURING

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: 376024300riskontrolSH
Device name: RISKONTROL tips
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: ACTEON MANUFACTURING
SRN: FR-MF-000007556
Country: France
Email: genevieve.devilledon@acteongroup.com
Phone: +33 6 03 04 65 64

Variants by status

UDI-DI variants

13 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

basicUdiUlid01FVCTANMSWTQ54F9TYH87B3B2

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

20170403760243000478
20170103760243000447
20170003760243000430
20170303760243000461
20170203760243000454
20166503760243000508
20166603760243000515
20166903760243001093
20166803760243000539
20166703760243000522
20166403760243000492
20175003760243000546
Total protec by RISKONTROL03760243000553