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.

Ortopedická obuv pre diabetikov — 24 UDI-DI variants, MDR

MD Atlas
Diawin s.r.o.

Data from EUDAMED, last updated May 31, 2026

Ortopedická obuv pre diabetikov

858602288AF16FT

24 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: Diawin s.r.o.

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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 858602288AF16FT
Device name: Ortopedická obuv pre diabetikov
Device model: Midnight Tulip
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Diawin s.r.o.
SRN: SK-MF-000048596
Country: Slovakia
Email: janura@diawin.de

Variants by status

UDI-DI variants

24 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

basicUdiUlid01K33YC34SCWTN3JM90YNEP5CV

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

AF1636308586022880391
AF1637108586022880407
AF1642108586022885259
AF1637208586022880414
AF1640108586022880490
AF1638208586022880445
AF1642208586022885266
AF1639208586022880476
AF1643108586022888229
AF1638308586022880452
AF1640308586022880513
AF1640208586022880506
AF1643208586022885105
AF1639108586022880469
AF1642308586022885273
AF1636208586022880384
AF1639308586022880483
AF1641308586022880544
AF1643308586022885112
AF1641108586022880520
AF1641208586022880537
AF1637308586022880421
AF1638108586022880438
AF1636108586022880377