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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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Universal Actuator Modules — 5 UDI-DI variants, MDR

MD Atlas
Focal Meditech BV

Data from EUDAMED, last updated May 30, 2026

Universal Actuator Modules

8720299756FOCUAMMQ

5 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: Focal Meditech BV

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8720299756FOCUAMMQ
Device name: Universal Actuator Modules
Device model: Rise Up
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: Focal Meditech BV
SRN: NL-MF-000000536
Country: Netherlands
Email: info@focalmeditech.nl
Phone: +31135333103

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HNZH704JQP2535DYGQW4BFFY

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

60019508720299756878
60691308720299756885
60838308721398039015
60838408720299756892
60838508721398039008