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Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN 29001
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN 29001
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN 29001
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN 29001
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9001
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9001
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN 29002
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN 29002
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN 29002
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN 29002
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9002
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9002
99.60 Withdrawal effective
Graphical symbols for use in the labelling of medical devices
99.60 Withdrawal effective
Graphical symbols for use in the labelling of medical devices
99.60 Withdrawal effective
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9001 (revision of EN 46001:1996) (identical to ISO 13485:1996)
99.60 Withdrawal effective
