Zakłady Farmaceutyczne Polpharma SA

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Officers and regulatory representatives of Zakłady Farmaceutyczne Polpharma SA

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
LTDR-0500-000	`LTDR-0500-000`	`05900257102685`	1	On the market
ALFR-0400-000	`ALFR-0400-000`	`05900257035891`	1	On the market

BARCZEWSKA Ewa
the technical documentation are drawn up and kept up-to-date;
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ŚWIĘCICKA Katarzyna
the technical documentation are drawn up and kept up-to-date;
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ZACHARSKA Jolanta
the technical documentation are drawn up and kept up-to-date;
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DUZOWSKA Agnieszka
the technical documentation are drawn up and kept up-to-date;
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LEWANDOWSKA Magdalena
the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released;
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HEBEL Aleksandra
the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released;
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RESZKE Karolina
the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released;
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KAŹMIERCZYK-GRUCA Małgorzata
the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released;
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KONIKOWSKA-KUZIEŃKO Anna
the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; the EU declaration of conformity are drawn up and kept up-to-date;
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SERAFIN Anna
- the post-market surveillance obligations are complied with in accordance with Article 10(10); - in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued. - the reporting obligations referred to in Articles 87 to 91 are fulfilled
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TRZEMŻALSKA - WŁADYKA Anna
the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released;
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PIETKIEWICZ Justyna
the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released;
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FIMOWICZ Aneta
the EU declaration of conformity are drawn up and kept up-to-date
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Certificate health for Zakłady Farmaceutyczne Polpharma SA

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Device catalog for Zakłady Farmaceutyczne Polpharma SA

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About Zakłady Farmaceutyczne Polpharma SA

Contact details for Zakłady Farmaceutyczne Polpharma SA

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Officers and regulatory representatives of Zakłady Farmaceutyczne Polpharma SA

Certificate health for Zakłady Farmaceutyczne Polpharma SA

Device catalog for Zakłady Farmaceutyczne Polpharma SA

Statistics for Zakłady Farmaceutyczne Polpharma SA

Market presence of Zakłady Farmaceutyczne Polpharma SA

Devices by risk class