Actors of the Medical Devices sector, you wish to analyze the inorganic residues on your products
The international standard ISO 19227 “Surgical Implants – Cleanliness of Orthopaedic Implants – General Requirements” is a guideline describing the requirements for the cleanliness of orthopaedic implants and the validation of the cleaning processes used.
The objective of cleaning validation via ISO 19227 is to verify the effectiveness of the cleaning process in reducing physical, chemical and microbiological contaminants below a customer-defined level.
Why analyze inorganic residues according to the 19227 standard?
Inorganic residues can have adverse effects on the durability of medical devices but also on their non-toxicity.
Therefore, the analysis of inorganic residues according to the 19227 standard, allows to verify the conformity of your medical devices and to put them on the market.
FILAB supports you in the analysis of inorganic residues according to the 19227 standard
FILAB laboratory offers a wide range of services, some of which are COFRAC ISO 17025 accredited (www.cofrac.fr), according to validated and documented methods, helping you to comply with the requirements of the ISO 19227 standard.
