Mise à jour EUDAMED : le 9 avr. 2024

HEMOFARM AD

RS-MF-000020482

Actif

Adresse: Beogradski put, b.b. 26300 Vršac
Rôle: Fabricant
Date d'enregistrement: 18 févr. 2022
Pays: Serbie

HEMOFARM AD est un fabricant de dispositifs médicaux enregistré dans EUDAMED. Son siège est situé à Vršac, Serbie. Découvrez son profil réglementaire, ses dispositifs et ses certificats sur MD Atlas.

Information sur HEMOFARM AD

: RS-MF-000020482
Rôle: Fabricant
Pays: Serbie
Nom de l'organisation: HEMOFARM AD
Numéro TVA UE: Non applicable
Registre du commerce: 08010536
Date d'enregistrement: 18 févr. 2022

Contact de HEMOFARM AD

Téléphone: +381 13 803 100
Email: medicinskasredstvadijetetikakozmetika@hemofarm.com
Site web: www.hemofarm.com
Adresse: B.B., BEOGRADSKI PUT 26300 VRŠAC SERBIE

Autorité compétente

Nom: Nemzeti Népegészségügyi és Gyógyszerészeti Központ

Téléphone: +36 1 886 9300
Email: amd@nngyk.gov.hu

Dirigeants et représentants réglementaires de HEMOFARM AD

MARINKOVIĆ Tamara
Ensuring 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
Masqué
TOT Ljubica
Ensuring 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
Masqué
TRIFU Gedja
Ensuring 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
Masqué
KOSOVAC Radivoj
Ensuring 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
Masqué
IVKOVIĆ Jelena
Ensuring 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
Masqué
OBRADOVIĆ Nada
Ensuring 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
Masqué
PETROVIĆ Nevena
Ensuring 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

HEMOFARM AD

Information sur HEMOFARM AD

Contact de HEMOFARM AD

Autorité compétente

Dirigeants et représentants réglementaires de HEMOFARM AD

Recherches associées

Information sur HEMOFARM AD

Contact de HEMOFARM AD

Autorité compétente

Dirigeants et représentants réglementaires de HEMOFARM AD

Statistique de HEMOFARM AD

Santé des certificats de HEMOFARM AD

Catalogue des dispositifs de HEMOFARM AD

Familles de dispositifs (IUD-ID de base) de HEMOFARM AD

Recherches associées

Santé des certificats de HEMOFARM AD

Statistique de HEMOFARM AD

Familles de dispositifs (IUD-ID de base) de HEMOFARM AD

Catalogue des dispositifs de HEMOFARM AD