Side Bending Short Reduction Forceps I

Nom de l'organisation

SRN

CN-MF-000004851

Statut du fabricant

Actif

1 avertissement enregistré — faire défiler le panneau pour tout voir.

• -To minimize the risk of infection, these devices must be cleaned and sterilized prior to the first use and after every subsequent use. -Assembled instruments will not clean or sterilize completely. Disassemble all instruments prior to cleaning and sterilization. -Using unspecified sterilization cycles or agents may damage the device or result in incomplete sterilization. -Wear appropriate protective equipment: gloves, eye protection, etc. -Clinical orthopedics with the qualification of vice-director physician or above (including vice-director physician) can use this product and give detailed medical advice to patients. -The products may be used in conjunction with other implants and supporting surgical instruments. The products from different manufactures should never be used together. -If tool wear or defect affects normal use, it should be prohibited.

  AUTRE

Marché principal en Pays-Bas ; disponible dans 1 pays au total.

• Numéro de lot
• Date d'expiration
• Date de fabrication
• Numéro de série
• Identification du logiciel

Nomenclature européenne des dispositifs médicaux — la classification produit UE attribuée à ce dispositif.

• L0922ORTHOPAEDIC SURGERY GUIDES, REUSABLE

• Dispositifs médicaux de Classe I dans EUDAMED

Aucun certificat ne référence l'IUD-ID de base de ce dispositif.