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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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Sala-Med Peroneus emelő — 6 UDI-DI variants, MDR

MD Atlas
Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.

Data from EUDAMED, last updated May 24, 2026

Sala-Med Peroneus emelő

5999571440009GM

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: Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5999571440009GM
Device name: —
Device model: Sala-Med Peroneus emelő
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.
SRN: HU-MF-000004191
Country: Hungary
Email: zsolt.jobai@salamed.hu
Phone: +36309424236

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KPWZKFR3AH5Z42R31ARNBA2Q

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

0599957144088705999571440887
0599957144089405999571440894
0599957144090005999571440900
0599957144085605999571440856
0599957144086305999571440863
0599957144087005999571440870