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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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schaerer® axis — 2 UDI-DI variants, MDR (Schaerer Medical AG)

MD Atlas
Schaerer Medical AG

Data from EUDAMED, last updated May 23, 2026

schaerer® axis

764014393AxisNN

2 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: Schaerer Medical AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764014393AxisNN
Device name: schaerer® axis
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: Schaerer Medical AG
SRN: CH-MF-000038078
Country: Switzerland
Email: info@schaerermedical.ch
Phone: +41317202200

Authorised representative

Name: Intelleg Management GmbH
SRN: DE-AR-000037613
Country: Germany
Phone: +49 172 6454758

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HCEZ6BFBTEN8QTHSHW35P3JA

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

schaerer® axis 50007640143930005
schaerer® axis 70007640143930029