Statistics for Ideal Partner

312Total Devices

5Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for Ideal Partner

No certificates registered for this manufacturer.

Showing 1–25 of 312 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
184110	`184110`	`05901157624734`	100	On the market
184210	`184210`	`05901157628206`	100	On the market
172210	`172210`	`05901157625427`	100	On the market
172110	`172110`	`05901157625441`	100	On the market
182210	`182210`	`05901157629753`	100	On the market
182110	`182110`	`05901157625403`	100	On the market
182310	`182310`	`05901157620989`	100	On the market
173200	`173200`	`05901157625502`	100	On the market
173100	`173100`	`05901157625526`	100	On the market
173101	`173101`	`05901157629760`	100	On the market
183110	`183110`	`05901157625489`	50	On the market
183210	`183210`	`05901157625465`	50	On the market
10311	`10311`	`05901157625632`	100	On the market
10310	`10310`	`05901157625656`	100	On the market
10313	`10313`	`05901157625670`	100	On the market
10120	`10120`	`05901157620491`	100	On the market
10110	`10110`	`05901157620767`	100	On the market
181200	`181200`	`05901157625212`	100	On the market
171900	`171900`	`05901157621870`	100	On the market
1011091	`1011091`	`05901157624444`	100	On the market
179100	`179100`	`05901157625083`	100	On the market
1791001	`1791001`	`05901157626585`	100	On the market
189201	`189201`	`05901157627490`	100	On the market
189100	`189100`	`05901157624994`	100	On the market
189101	`189101`	`05901157620798`	100	On the market

Devices placed in 1 country

EUDAMED update: May 22, 2025

PL-MF-000047903

Active

SRN: PL-MF-000047903
Role: Manufacturer
Country: Poland
Organization name: Ideal Partner Spółka z ograniczoną odpowiedzialnością Spółka komandytowa
EU VAT number: 5422485241
EORI: PL542248524100000
Trade register: 0000628325
Date of registration: May 20, 2025

DOJLIDKO Jakub
Responsible for ensuring compliance with the technical documentation, EU declaration of conformity, post-market surveillance, vigilance reporting, and clinical investigation obligations in accordance with Article 15 of Regulation (EU) 2017/745 (MDR).
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