• Validation summary guide

ReNu SU Technology cartridge validation summary guide

ReNu SU Technology cartridges

ReNu SU Technology and its raw materials have been tested under a range of pharmacopoeial and non-pharmacopoeial standards. These include:

  • USP Biocompatibility in vivo and in vitro
  • European Pharmacopoeia, 3.1.9
  • ISO 10993

Additional testing carried out includes extractables testing.

The full validation guide including additional information regarding test methods and actual test reports is available on request.

ReNu SU Technology, its raw materials and manufacturing process meets a number of regulatory compliance legislations. Specific statements relating to these compliances are available in the ReNu SU Technology compliance guide.

Both the full validation guide and the compliance guide can be requested by submitting the below form.

renu validation guide,

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ReNu SU Technology cartridge validation summary guide

Validation summary guide PDF - 367kb

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Thank you for requesting our validation documentation. We have received your request and will respond within 48 hours.

Disclaimer: You hereby agree the provided validation guide is for private use only to assist in the qualification of the products listed within the validation guide.

You also agree that you will not copy, redistribute, transmit, assign, sell, broadcast, rent, share, lend, modify, adapt, edit or transfer the validation guide to any other party without prior consent from WMFTS.

Disclaimer: You hereby agree the provided validation guide is for private use only to assist in the qualification of the products listed within the validation guide.

You also agree that you will not copy, redistribute, transmit, assign, sell, broadcast, rent, share, lend, modify, adapt, edit or transfer the validation guide to any other party without prior consent from WMFTS.