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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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Ortho Rehab 3 — 415 UDI-DI variants, MDR (Künzli SwissSchuh AG)

MD Atlas
Künzli SwissSchuh AG

Data from EUDAMED, last updated May 23, 2026

Ortho Rehab 3

76300428Stabilschuhe5M

415 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: Künzli SwissSchuh AG

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Device characteristics

Animal tissues / cells

Identity & classification

Basic UDI-DI: 76300428Stabilschuhe5M
Device name: Ortho Rehab 3
Device model: Stabilschuhe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Künzli SwissSchuh AG
SRN: CH-MF-000044954
Country: Switzerland
Email: info@kuenzli-schuhe.ch
Phone: +41 56 200 85 00

Authorised representative

Name: Axxos GmbH
SRN: DE-AR-000005590
Country: Germany
Phone: +41795637850

Variants by status

UDI-DI variants

415 UDI-DI variants

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Applied filters

basicUdiUlid01JXF3SRPCFVNY89XHEJE1MQPJ

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

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