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.

Skarpetki zdrowotne profilaktyczne — 12 UDI-DI variants, MDR

MD Atlas
JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin

Data from EUDAMED, last updated May 30, 2026

Skarpetki zdrowotne profilaktyczne

5901050DMWool36

12 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: JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin

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: 5901050DMWool36
Device name: Skarpetki zdrowotne profilaktyczne
Device model: DEOMED WOOL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 31, 2024

Manufacturer & authorised representative

Manufacturer

Name: JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin
SRN: PL-MF-000009541
Country: Poland
Email: info@jjw.pl
Phone: +48 22 711 71 58

Variants by status

UDI-DI variants

12 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

basicUdiUlid01HNFTKZP213JXANP88ZFVSCKH

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

DMW05901050201827
DMW05901050201926
DMW05901050201629
DMW05901050209625
DMW05901050201728
DMW05901050202725
DMW05901050202824
DMW05901050209823
DMW05901050202626
DMW05901050209724
DMW05901050209922
DMW05901050202923