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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Activmotion S DTO — 2 UDI-DI variants, MDR (Newclip Technics SAS)

MD Atlas
Newclip Technics SAS

Data from EUDAMED, last updated May 19, 2026

Activmotion S DTO

3700569600158V

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Newclip Technics SAS

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 3700569600158V
Device name: Activmotion S DTO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Newclip Technics SAS
SRN: FR-MF-000011809
Country: France
Email: regulatory@newcliptechnics.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K954M8K40R9DF91648121GJN

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

FTPS1-ST03700569629564
FTPS2-ST03700569629588