Model Catalog: D 3446 (Lot serial: consult with manufacturer); Model Catalog: D 3344 (Lot serial: consult with manufacturer); Model Catalog: D 3446 (Lot serial: various); Model Catalog: D 3344 (Lot serial: various)
Model Catalog: (Lot serial: 40215); Model Catalog: (Lot serial: 40089); Model Catalog: (Lot serial: 40152); Model Catalog: (Lot serial: 40091); Model Catalog: (Lot serial: 40218); Model Catalog: (Lot serial: 40232); Model Catalog: (Lot serial: 20120); Model Catalog: (Lot serial: 40105); Model Catalog: (Lot serial: 40118); Model Catalog: (Lot serial: 40161); Model Catalog: (Lot serial: 40172); Model Catalog: (Lot serial: 20137); Model Catalog: (Lot serial: 40034); Model Catalog: (Lot serial: 40039); Model Catalog: (Lot serial: 40064); Model Catalog: (Lot serial: 40081); Model Catalog: (Lot serial: 40201); Model Catalog: (Lot serial: 20028); Model Catalog: (Lot serial: 20135); Model Catalog: (Lot serial: 40053); Model Catalog: (Lot serial: 40055); Model Catalog: (Lot serial: 40142); Model Catalog: (Lot serial: 40170); Model Catalog: (Lot serial: 40088)
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.