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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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Solatronic SL-3 — 1 UDI-DI variant, MDR

MD Atlas
Elektronika i Elektromedycyna M.Lewandowski Sp.J.

Data from EUDAMED, last updated May 31, 2026

Solatronic SL-3

5906660092SL3CS

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Elektronika i Elektromedycyna M.Lewandowski Sp.J.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5906660092SL3CS
Device name: Solatronic SL-3
Device model: Solatronic SL-3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Elektronika i Elektromedycyna M.Lewandowski Sp.J.
SRN: PL-MF-000032400
Country: Poland
Email: office@eie.com.pl
Phone: +48227100839

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KKEJVHSE79SK7CJMTKDCTFX3

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

Solatronic SL-305906660092032