Statistics for "Masters" Sp. z o.o.

8Total Devices

8Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for "Masters" Sp. z o.o.

No certificates registered for this manufacturer.

Devices by risk class

Device catalog for "Masters" Sp. z o.o.

Showing 1–8 of 8 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
-	`-`	`05906761200244`	1	On the market
-	`-`	`05906761200657`	1	On the market
-	`-`	`05906761200664`	1	On the market
-	`-`	`05906761200275`	1	On the market
-	`-`	`05906761200640`	1	On the market
-	`-`	`05906761200213`	1	On the market
-	`-`	`05906761200077`	1	On the market
-	`-`	`05906761200633`	1	On the market

Device families (Basic UDI-DI) of "Masters" Sp. z o.o.

Showing 1–8 of 8 device families.

Market presence of "Masters" Sp. z o.o.

Devices placed in 1 country

Poland8

MD Atlas update: May 31, 2026

"Masters" Sp. z o.o.

PL-MF-000030292

Active

Address: Skórzewska, 30 62-081 Wysogotowo
Role: Manufacturer
Date of registration: Nov 3, 2022
Country: PL Poland

About "Masters" Sp. z o.o.

SRN: PL-MF-000030292
Role: Manufacturer
Country: Poland
Organization name: "Masters" Sp. z o.o.
EU VAT number: 782-00-68-236
EORI: PL782006823600000
Trade register: 0000191642
Date of registration: Nov 3, 2022

Contact details for "Masters" Sp. z o.o.

Address: 30, SKÓRZEWSKA 62-081 WYSOGOTOWO POLAND
Email: rzadkowska@masters.poznan.pl

Validator

Name: Urząd Rejestracji Produktów Leczniczych
SRN: PL-CA-014
Phone: +48 22 492 11 71
Email: wm@urpl.gov.pl

Officers and regulatory representatives of "Masters" Sp. z o.o.

RZĄDKOWSKA Mariola
the conformity of the devices is appropriately checked, IAW the quality management system under which they are produced, before a device is released the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the post-market surveillance obligations are complied with IAW Art10(10) the reporting obligations referred to in Art87-91 are fulfilled; in the case of investigational devices, the statement referred to in Section 4.1 of Chpt II of Annex XV is issued
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