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.

Proteza Piersi Maxima — 284 UDI-DI variants, MDR

MD Atlas
PRZEDSIĘBIORSTWO OBROTU I FABRYKACJI ARTYKUŁÓW MEDYCZNYCH "POFAM- POZNAŃ" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data from EUDAMED, last updated May 31, 2026

Proteza Piersi Maxima

59041250BREASTPROSTHES73

284 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: PRZEDSIĘBIORSTWO OBROTU I FABRYKACJI ARTYKUŁÓW MEDYCZNYCH "POFAM- POZNAŃ" 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: 59041250BREASTPROSTHES73
Device name: Proteza Piersi Maxima
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: PRZEDSIĘBIORSTWO OBROTU I FABRYKACJI ARTYKUŁÓW MEDYCZNYCH "POFAM- POZNAŃ" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
SRN: PL-MF-000050850
Country: Poland
Email: office@pofam.poznan.pl
Phone: +48618342309

Variants by status

UDI-DI variants

284 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

basicUdiUlid01KR68A69FXDG576DJ1SMFHWCP

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

9006-L-T0805904125002930
8005-E-T2005904125002336
7004-C-PRAWA-T0105904125000516
7004-L-PRAWA-T1205904125000950
4001-T1705904125001179
4001-T0205904125001025
7004-C-LEWA-T0605904125000400
7004-LEWA-T1205904125000134
4001-U-T0305904125001810
7004-C-LEWA-T1205904125000462
7004-LEWA-T0305904125000042
7004-L-PRAWA-T005904125000837
8005-E-T1205904125002251
8005-L-T1305904125001520
7004-C-PRAWA-T0305904125000530
4001-T0605904125001063
4001-T0405904125001049
9006-L-T0605904125002916
7004-L-PRAWA-T0805904125000912
7004-PRAWA-T1105904125000295
8005-L-T2005904125001599
4001-L-T0705904125001674
7004-C-LEWA-T1405904125000486
7004-C-LEWA-T0805904125000424
8005-E-T1805904125002312

4 5 6 7 8