ARTHREX INC

2 dispositifs dans la base de données

  • Modèle / numéro de série
    Model Catalog: (Lot serial: 13258)
  • Modèle / numéro de série
    Model Catalog: AR-2600SBS-7 (Lot serial: batch# 10081420); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10081420); Model Catalog: AR-2600SBS-7 (Lot serial: batch# 10076852); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10076852); Model Catalog: AR-2600SBS-7 (Lot serial: batch# 10076753); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10076753); Model Catalog: AR-2600SBS-7 (Lot serial: batch# 10084027); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10084027); Model Catalog: AR-2600SBS-7 (Lot serial: batch# 10074288); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10074288); Model Catalog: AR-2600SBS-7 (Lot serial: batch# 10074291); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10074291); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10075965); Model Catalog: AR-2600SBS-7 (Lot serial: batch# 10075965); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10077252); Model Catalog: AR-2600SBS-7 (Lot serial: batch# 10077252); Model Catalog: AR-2600SBS-5 (Lot serial: batch# 10070003); Model Catalog: AR-26
  • Description du dispositif
    SPEEDBRIDGE IMPLANT SYSTEM With BIOCOMPOSITE SWIVELOCK SP (SHOULDER);PEEK SWIVELOCK SELF-PUNCHING;BIO-COMPOSITE SWIVELOCK SELF-PUNCHING;BIO-SWIVELOCK SELF-PUNCHING

6 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
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