Documents
Quality, regulatory & legal documentation
Access our certification and governance documents. For technical files and product-specific IFUs, please contact info@craniotech.ir.
ISO 13485:2016 CertificateCertification for the design and manufacture of patient-specific implants.Download PDF ↓Warranty & Limitations of LiabilityTerms governing the supply and use of CranioTech patient-matched devices.Download PDF ↓PAIA ManualPromotion of Access to Information Act manual, as required in South Africa.Download PDF ↓Instructions for Use (IFU)General handling, cleaning and sterilisation guidance for CranioTech devices.Download PDF ↓
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