Statistique de Stryker GmbH

7Dispositifs total

3UDI-DI de base

0Non destinés au marché UE

0Certificats

0Valides

0Expirant < 6 mois

1Pays

Santé des certificats de Stryker GmbH

Aucun certificat enregistré pour ce fabricant.

Affichage de 1–7 sur 7 dispositifs.

Dénomination commerciale	Numéro de référence/catalogue	Code d'UDI-DI	Quantité	Statut
4935-9-940	`4935-9-940`	`07613327294248`	1	Sur le marché
629590S	`629590S`	`07613327131512`	1	Sur le marché
629579S	`629579S`	`07613327131468`	1	Sur le marché
629589S	`629589S`	`07613327131499`	1	Sur le marché
629589	`629589`	`07613327131444`	1	Sur le marché
629579	`629579`	`07613327131567`	1	Sur le marché
629590	`629590`	`07613327131536`	1	Sur le marché

Dispositifs placés dans 1 pays

Mise à jour MD Atlas : le 27 mai 2026

CH-MF-000009332

Actif

REDDEN Jeanine
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Masqué
STAP Dannielle
Ensuring that the post-market surveillance obligations are complied with in accordance with Article 10(10) of the EU MDR. Ensuring that the reporting obligations referred to in Articles 87 to 91 of the EU MDR are fulfilled.
Masqué
PARRISH Matthew
Ensuring that 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