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.

Veera Mikrofibra Premium 70 den ucisk… — 1 UDI-DI variant, MDR

MD Atlas
Kati spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

Veera Mikrofibra Premium 70 den ucisk 13-17 mmHg Rajstopy uciskowe

590336461VM70ED

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Kati spółka z ograniczoną odpowiedzialnością

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: 590336461VM70ED
Device name: Veera Mikrofibra Premium 70 den ucisk 13-17 mmHg Rajstopy uciskowe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: Kati spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000036162
Country: Poland
Email: info@kati.pl
Phone: +48 601353826

Variants by status

UDI-DI variants

1 UDI-DI variant

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

basicUdiUlid01H8BQ9Z0ZSRNQQ5JT0YX2PWNG

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

VM7005903364614737