Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

4559507630042808536
Y06330307630042810508
4595907630042808475
4559507630042808512
4559507630042808444
4559507630042808529
4559507630042808611
4559507630042808482
4559507630042808499
4559507630042808567
4559507630042808598
4559507630042808581
4559507630042810492
4559507630042808543
4559507630042808550
4559507630042808468
4559507630042808505
4559507630042808437
4559507630042808451
4558107630042807607
4558107630042807720
4558107630042807621
4558107630042807744
4558107630042807706
4558107630042807584