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

7004-C-PRAWA-T0205904125000523
7004-L-PRAWA-T0605904125000899
9006-U-T1505904125002664
7004-PRAWA-T0305904125000219
7004-C-LEWA-T0105904125000356
8005-T2005904125001384
8005-L-T1205904125001513
9006-U-T1405904125002657
7004-L-PRAWA-T0405904125000875
8005-T1005904125001285
4001-L-T0905904125001698
4001-W-T1705904125002121
8005-E-T1905904125002329
8005-E-T1505904125002282
4001-L-T0205904125001629
4001-L-T1605904125001766
9006-L-T1405904125002992
4001-W-T0505904125002008
8005-E-T0705904125002206
8005-T0505904125001230
9006-T0805904125002428
4001-L-T005904125001605
7004-C-LEWA-T0205904125000363
7004-LEWA-T0105904125000028
4001-T1005904125001100