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.

NON-INVASIVE DISPOSABLE INSTRUMENTS — 49 UDI-DI variants, MDR

MD Atlas
TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

Data from EUDAMED, last updated May 31, 2026

NON-INVASIVE DISPOSABLE INSTRUMENTS

5900516BBCXXXXSK

49 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: 5900516BBCXXXXSK
Device name: NON-INVASIVE DISPOSABLE INSTRUMENTS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 29, 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

49 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

basicUdiUlid01KG4Q5FBB3K1QJN698ZFZ8NGT

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

MA-291-PAT1-00805900516845728
MA-291-PAT1-02605900516873196
MA-291-DREN-00205900516331757
MA-291-KLE1-03705900516865429
MA-291-POJ1-02805900516867454
MA-PR0-7023-00205900516275365
MA-291-POJ1-03205900516333669
MA-291-POJ1-00405900516848729
MA-291-PAT1-00305900516841164
MA-291-POJ1-02905900516867805
MA-291-POJ1-01605900516853372
MB-291-POJ1-02605900516866495
MA-291-PAT1-02105900516866709
MA-291-POJ1-00605900516848743
MA-291-KLE1-00105900516842345
MA-291-POJ1-02205900516866051
MA-291-PAT1-02505900516873073
MA-PR0-7023-00105900516275358
MA-291-PENS-01805900516865474
MA-291-POJ1-01005900516852610
MA-291-PAT1-01505900516863791
MB-291-POJ1-02505900516866488
MB-291-POJ1-02705900516866501
MA-291-POJ1-00705900516852214

1 2