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.

GYNAECOLOGICAL TOWELS AND ABSORBENT… — 9 UDI-DI variants, MDR

MD Atlas
TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

Data from EUDAMED, last updated May 30, 2026

GYNAECOLOGICAL TOWELS AND ABSORBENT INSERTS NON STERILE

5900516AAHXXXXTC

9 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: TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

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: 5900516AAHXXXXTC
Device name: GYNAECOLOGICAL TOWELS AND ABSORBENT INSERTS NON STERILE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
SRN: PL-MF-000002200
Country: Poland
Email: biuro.zarzadu@tzmo-global.com
Phone: +48 56 612 39 00

Variants by status

UDI-DI variants

9 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

basicUdiUlid01KGMJR5S3SHFSMSDZ5B3C4ZMQ

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

BE-139-N010-02105900516841126
BE-139-N010-00305900516897802
BE-139-N015-00405900516858377
BE-139-N010-02005900516867164
BE-139-N010-00205900516893439
BE-139-N020-00305900516025786
BE-139-N020-00405900516025793
BE-139-N010-01105900516894894
BE-139-N010-00705900516893446