Mise à jour EUDAMED : le 9 avr. 2026

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

PL-AR-000020080

MandataireActif

Adresse: Aleja Colgate, 2 58-100 Świdnica
Rôle: Mandataire
Date d'enregistrement: 9 févr. 2022
Pays: Pologne

Colgate-Palmolive Manufacturing (Poland) sp. z o.o. est un mandataire européen enregistré dans EUDAMED. Son siège est situé à Świdnica, Pologne. Découvrez son profil réglementaire, ses dispositifs et ses certificats sur MD Atlas.

Information sur CP

: PL-AR-000020080
Rôle: Mandataire
Pays: Pologne
Nom de l'organisation: Colgate-Palmolive Manufacturing (Poland) sp. z o.o.
Numéro TVA UE: 5272484500
EORI: PL527248450000000
Registre du commerce: 0000240496
Date d'enregistrement: 9 févr. 2022

Contact de CP

Téléphone: +48 74 856 7000
Email: meddev_eurep@colpal.com
Site web: www.colgate.com
Adresse: 2, ALEJA COLGATE 58-100 ŚWIDNICA POLOGNE

Dirigeants et représentants réglementaires de 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
Masqué
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;
Masqué
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
Masqué

Autorité compétente

Nom: Urząd Rejestracji Produktów Leczniczych

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

Recherches associées

Rôle et obligations dans EUDAMED

Un mandataire est une entité établie dans l’Espace économique européen qu’un fabricant établi hors de l’EEE désigne pour agir en son nom pour des tâches réglementaires déterminées. L’enregistrement dans EUDAMED est obligatoire en vertu de l’article 11 du règlement (UE) 2017/745 et de l’article 11 du règlement (UE) 2017/746.

Dirigeants et représentants réglementaires de 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
Masqué
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;
Masqué
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
Masqué

Rôle et obligations dans EUDAMED

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

Rôle et obligations dans EUDAMED

Fabricants hors UE représentés

Rôle et obligations dans EUDAMED

Fabricants hors UE représentés