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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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SOLIS 60 Lampa zabiegowe — 6 UDI-DI variants, MDR

MD Atlas
FAE Famed Łódź S.A.

Data from EUDAMED, last updated May 30, 2026

SOLIS 60 Lampa zabiegowe

5904708713SOLIS60X9

6 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: FAE Famed Łódź S.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5904708713SOLIS60X9
Device name: SOLIS 60 Lampa zabiegowe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 7, 2023

Manufacturer & authorised representative

Manufacturer

Name: FAE Famed Łódź S.A.
SRN: PL-MF-000018775
Country: Poland
Email: info@famed.pl

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H9QEKD5YKF2AKBBPRYBX9WTB

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

SOLIS 60 C05904708713161
SOLIS 60 F05904708713178
SOLIS 60 W05904708713154
SOLIS 60/60 C05904708713185
SOLIS 60/60 F05904708713192
SOLIS 60*60 W05904708713208