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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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SafeFix — 6 UDI-DI variants, MDR (MSP Medizintechnik GmbH)

MD Atlas
MSP Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

SafeFix

912004788HSOSAFIX6A

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: MSP Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 912004788HSOSAFIX6A
Device name: SafeFix
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: MSP Medizintechnik GmbH
SRN: AT-MF-000018341
Country: Austria
Email: info@hso-solutions.at

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01G9YSHW32RG0358G7KK8ZDTSJ

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

HSOSAFIX300009120047883310
HSOSAFIX200009120047883297
HSOSAFIX100009120047883273
HSOSAFIX500009120047880395
HSOSAFIX5000L09120047883112
HSOSAFIX400009120047883068