Disposable Linear Staplers and cartridges

Dénomination commerciale

Disposable Linear Staplers and cartridges

Code d'IUD-ID

06954790940050

IUD-ID de base

B-06954790940050

Numéro de référence/catalogue

TCYZ-30×3.8

Entité d'attribution

GS1

Catégorie de risque

Classe IIb

Législation applicable

MDD [Directive 93/42/CEE relative aux dispositifs médicaux]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

—

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

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

• H02020199LINEAR STAPLERS FOR OPEN SURGERY - OTHER

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

• CW999

  1.The stapler is disposable and can be used after opening the sterile package. Once the package is found to be damaged, it must not be used. When in use, the sterile techique shall be strictly executed. 2.The stapler is sterilized by ethylene oxide, and is delivered in a sterile sealed package. The validity period is three years from the date of sterilization. Products beyond the validity period are strictly prohibited to use. 3.When the stapler is completely closed, the thickness of the suture cartridge is between 1.0 and 2.5 mm. 4.When the stapler is released, if it does not reset, you should first push the cartridge to reset it, and then pull the locating rod handle to the final position. 5.Before the tissue stapling operation, the locating rod must be inserted into the locating hole of the anvil. 6.After withdrawing the stapler, be sure to check the staple line for hemostasis. If there is bleeding, electrocautery or suturing of a few stitches is required in the corresponding part. 7.These Instructions only give a general introduction to the use of the stapler, and are not used for operation guidance. The operator must refer to other relevant medical documents and relevant operation maps during the operation.

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