UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

JSA - JIS T 3250

Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

active, Most Current
Buy Now
Organization: JSA
Publication Date: 1 March 2013
Status: active
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

JIS T 3250
March 1, 2022
Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
A description is not available for this item.
JIS T 3250
March 1, 2013
Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
A description is not available for this item.
JIS T 3250
July 29, 2011
Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
A description is not available for this item.
JIS T 3250
March 25, 2005
Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
A description is not available for this item.

References

This document references:
ISO 10993-11 FRENCH - Évaluation biologique des dispositifs médicaux - Partie 11: Essais de toxicité systémique
Published by ISO on September 1, 2017
A description is not available for this item.
This document references:
JIS T 0307 - Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied
Published by JSA on September 25, 2004
A description is not available for this item.
This document references:
JIS T 0993-1 - Biological evaluation of medical devices -- Part 1: Evaluation and testing within a risk management process
Published by JSA on January 1, 2020
A description is not available for this item.
This document references:
ISO 10993-11 - Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
Published by ISO on September 1, 2017
This document specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
This document is referenced by:
JIS T 3248 - Extracorporeal blood circuit
Published by JSA on March 1, 2022
A description is not available for this item.
View Less
View All
Advertisement