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.

Szkiełka — 18 UDI-DI variants, IVDR

MD Atlas
Mar-Four Siekierska, Titienko S.C.

Data from EUDAMED, last updated May 31, 2026

Szkiełka

590572343605E6

18 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Mar-Four Siekierska, Titienko S.C.

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: 590572343605E6
Device name: Szkiełka
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Mar-Four Siekierska, Titienko S.C.
SRN: PL-MF-000036041
Country: Poland
Email: info@marfour.com.pl
Phone: +48 42 650 88 21

Variants by status

UDI-DI variants

18 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

basicUdiUlid01K8TB9PQ07B2Q344CXAJ5WKVQ

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

4L.0340-0120E05905723436714
4L.0340-0620E05905723436721
4L.0340-1620E05905723436745
4L.0340-2820E05905723436752
4L.0340-3220E05905723436769
4P.45.01667W05905723436295
4P.45.01667V05905723436301
4P.45.01667B05905723436318
4P.45.01667O05905723436325
4P.45.01667P05905723436332
4P.45.01667G05905723436349
4P.45.01667Y05905723436356
4P.90.01667W05905723436363
4P.90.01667B05905723436370
4P.90.01667O05905723436417
4P.90.01667P05905723436387
4P.90.01667G05905723436394
4P.90.01667Y05905723436400