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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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Actuator Keypad — 8 UDI-DI variants, MDR (mo-vis bv)

MD Atlas
mo-vis bv

Data from EUDAMED, last updated May 23, 2026

Actuator Keypad

540700832ACTKEYP9J

8 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: mo-vis bv

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 540700832ACTKEYP9J
Device name: Actuator Keypad
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: mo-vis bv
SRN: BE-MF-000000729
Country: Belgium
Email: rebecca.vancraeymeersch@mo-vis.com
Phone: +3293352860

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JQ9EAPTFV8SY4AQK5S0TVFBM

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

Actuator Keypad Button R-net CJSM105407008320133
Actuator Keypad Button Rnet CJSM205407008320157
Actuator Keypad Paddle Rnet CJSM105407008320140
Actuator Keypad Paddle Rnet CJSM205407008320164
Actuator Keypad PRO Button Rnet CJSM105407008320737
Actuator Keypad PRO Button Rnet CJSM205407008320751
Actuator Keypad PRO Paddle Rnet CJSM105407008320744
Actuator Keypad PRO Paddle Rnet CJSM205407008320768