PRICES include / exclude VAT
Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.40 Implants for surgery, prosthetics and orthotics>BS EN ISO 7197:2009 Neurosurgical implants. Sterile, single-use hydrocephalus shunts and components
immediate downloadReleased: 2009-10-31
BS EN ISO 7197:2009 Neurosurgical implants. Sterile, single-use hydrocephalus shunts and components

BS EN ISO 7197:2009

Neurosurgical implants. Sterile, single-use hydrocephalus shunts and components

Format
Availability
Price and currency
English Secure PDF
Immediate download
195.00 USD
You can read the standard for 1 hour. More information in the category: E-reading
Reading the standard
for 1 hour
19.50 USD
You can read the standard for 24 hours. More information in the category: E-reading
Reading the standard
for 24 hours
58.50 USD
English Hardcopy
In stock
195.00 USD
Standard number:BS EN ISO 7197:2009
Pages:16
Released:2009-10-31
ISBN:978 0 580 68136 3
Status:Standard
DESCRIPTION

BS EN ISO 7197:2009


This standard BS EN ISO 7197:2009 Neurosurgical implants. Sterile, single-use hydrocephalus shunts and components is classified in these ICS categories:
  • 11.040.40 Implants for surgery, prosthetics and orthotics

This International Standard specifies safety and performance requirements for sterile, single-use non-active hydrocephalus shunts and components. This includes the components used in shunts, like valves, tubes and reservoirs.

This International Standard gives no recommendation concerning the superiority of a certain type of valve.

For manufacturing, it defines the mechanical and technical requirements. This International Standard defines the technical information of the valve, to be given by the manufacturer. In respect to the different principles of the valve types, specific characteristics are defined for each group as declared by the manufacturer.

The benefit of this International Standard for the surgeon and the patient is to understand the information given by the manufacturer and to obtain standardized information about the performance of a well working product with new design characteristics. The benefit for the manufacturer is to define the important requirements for shunts as a basis for investigations during development as well as for quality control during manufacture.

This International Standard does not apply to active implants for the treatment of hydrocephalus.