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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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evoStim — 8 UDI-DI variants, MDR (BEACMED S.R.L.)

MD Atlas
BEACMED S.R.L.

Data from EUDAMED, last updated May 31, 2026

evoStim

805901671EVOSTIMVV

8 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: BEACMED S.R.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805901671EVOSTIMVV
Device name: evoStim
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: BEACMED S.R.L.
SRN: IT-MF-000023616
Country: Italy
Email: info@beacmed.eu
Phone: +39038543378

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JR8EEEXHHSV98R7SAYXM24ZR

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

evoStimE-00108059016710931
evoStimE-00208059016711341
evoStimK-00108059016710993
evoStimP-00108059016710948
evoStimP-00208059016711297
evoStimT-00108059016710955
evoStimUG-00108059016710962
evoStimUG-00208059016711358