Chengdu Puth Medical Technology Co., Ltd.

• DE/CA05 - Behorde fur Justiz und Verbraucherschutz
  AllemagneContacter l’autorité →

Aucun certificat enregistré pour ce fabricant.

Dispositifs placés dans 2 pays

• Italie187
• Allemagne117

4 contacts identifiés

• KY
  KANG Yu

  PCVRR
  Voir le profil →
• TL
  TANG Li

  PCVRR
  Voir le profil →
• TANG Li
  MDR and IVDR 1. Ensure the technical documents and EU conformity declarations are developed and kept up-to-date. 2. A statement is issued regarding the devices used in clinical trials, stating that "in addition to the aspects involved in clinical trials, the devices comply with general safety and performance requirements, and preventive measures have been taken to protect the health and safety of users.
  Masqué
• KANG Yu
  MDR and IVDR 1. Before releasing the device, check the conformity and consistency of product quality according to the requirements of the quality management system. 2. Comply with post market supervision obligations, implement and maintain the latest post market supervision procedures for products; 3. Fulfill the obligation of reporting medical devices, including reporting and analyzing serious accidents and on-site safety corrective measures, trend reporting, and implementation measures.
  Masqué

• Shanghai International Holding Corp. GmbH(Europe) — représente — PUTH
• KANG Yu — PUTH
• TANG Li — PUTH