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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Podwójna piłka EPP — 7 UDI-DI variants, MDR (4FIZJO GROUP SP. Z O. O.)

MD Atlas
4FIZJO GROUP SP. Z O. O.

Data from EUDAMED, last updated May 30, 2026

Podwójna piłka EPP

590773931DOUBLEEPPBALLM2

7 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: 4FIZJO GROUP SP. Z O. O.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590773931DOUBLEEPPBALLM2
Device name: Podwójna piłka EPP
Device model: Podwójna piłka EPP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2024

Manufacturer & authorised representative

Manufacturer

Name: 4FIZJO GROUP SP. Z O. O.
SRN: PL-MF-000031702
Country: Poland
Email: kontakt@4fizjo.pl
Phone: +48 570 071 575

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HY2KSBY8G9FMPG5WH37X54BZ

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

P-590722293134905907222931349
P-590722293130105907222931301
P-590722293133205907222931332
P-590773931480205907739314802
P-590722293131805907222931318
P-590722293129505907222931295
P-590722293132505907222931325