EUDAMED update: Apr 9, 2026

Colgate-Palmolive Manufacturing (Poland) sp. z o.o.

PL-AR-000020080

Authorised representativeActive

Address: Aleja Colgate, 2 58-100 Świdnica
Role: Authorised representative
Date of registration: Feb 9, 2022
Country: Poland

Colgate-Palmolive Manufacturing (Poland) sp. z o.o. is an EU authorised representative registered in EUDAMED. Headquartered in Świdnica, Poland. Explore the regulatory profile, devices and certificates on MD Atlas.

About CP

: PL-AR-000020080
Role: Authorised representative
Country: Poland
Organization name: Colgate-Palmolive Manufacturing (Poland) sp. z o.o.
EU VAT number: 5272484500
EORI: PL527248450000000
Trade register: 0000240496
Date of registration: Feb 9, 2022

Contact details for CP

Phone: +48 74 856 7000
Email: meddev_eurep@colpal.com
Website: www.colgate.com
Address: 2, ALEJA COLGATE 58-100 ŚWIDNICA POLAND

Officers and regulatory representatives of CP

JABLONSKA Hanna
-Verify that EU DoC and TD -Keep copy of TD, EU DoC & copy of certificate -Be registered and update the information in EUDAMED -Verify that manufacturer complied with registration obligations -Provide CA with all the information & documentation to demonstrate conformity -Forward to manufacturer request made by CA -Cooperate with CAs on preventive or corrective action -Immediately inform manufacturer about complaints & reports -Terminate mandate if manufacturer acts contrary to its obligations
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MATUSZCZYK Arleta
- Be registered and update the information in EUDAMED within a period of one month following a change to this information, confirm the validity of the information one year after submitting it and every second year thereafter - Verify that the manufacturer has complied with the registration obligations that the information is accurate, complete and up to date; - Cooperate with the CAs on any preventive or corrective action to eliminate or mitigate the risks posed by devices;
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MISLIN Ines
- Provide CA with all the information & documentation to demonstrate conformity; - Cooperate with the CAs on any preventive or corrective action to eliminate or mitigate the risks posed by devices; - Immediately inform the manufacturer about complaints and reports from HCP, patients and users about suspected incidents related to a device
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Competent authority

Name: Urząd Rejestracji Produktów Leczniczych

Phone: +48 22 492 11 71
Email: wm@urpl.gov.pl

Role and obligations in EUDAMED

An authorised representative is an entity established in the European Economic Area that a manufacturer based outside the EEA appoints to act on its behalf for specified regulatory tasks. Registration in EUDAMED is required under Article 11 of the MDR (2017/745) and Article 11 of the IVDR — règlement (UE) 2017/746.

Officers and regulatory representatives of CP

JABLONSKA Hanna
-Verify that EU DoC and TD -Keep copy of TD, EU DoC & copy of certificate -Be registered and update the information in EUDAMED -Verify that manufacturer complied with registration obligations -Provide CA with all the information & documentation to demonstrate conformity -Forward to manufacturer request made by CA -Cooperate with CAs on preventive or corrective action -Immediately inform manufacturer about complaints & reports -Terminate mandate if manufacturer acts contrary to its obligations
Hidden
MATUSZCZYK Arleta
- Be registered and update the information in EUDAMED within a period of one month following a change to this information, confirm the validity of the information one year after submitting it and every second year thereafter - Verify that the manufacturer has complied with the registration obligations that the information is accurate, complete and up to date; - Cooperate with the CAs on any preventive or corrective action to eliminate or mitigate the risks posed by devices;
Hidden
MISLIN Ines
- Provide CA with all the information & documentation to demonstrate conformity; - Cooperate with the CAs on any preventive or corrective action to eliminate or mitigate the risks posed by devices; - Immediately inform the manufacturer about complaints and reports from HCP, patients and users about suspected incidents related to a device
Hidden

Role and obligations in EUDAMED

Colgate-Palmolive Manufacturing (Poland) sp. z o.o.

Role and obligations in EUDAMED

Non-EU manufacturers represented

Role and obligations in EUDAMED

Non-EU manufacturers represented