---
type: "WebPage"
title: "Inorganic residue analysis according to ISO 19227"
description: "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..."
resource: "https://filab.fr/en/our-services/our-expertise-services/laboratory-analyis-standard-iso-19227/inorganic-residue-analysis-according-to-iso-19227/"
tags: ["EN", "pll_62bd4d065c5fb", "Anaïs DECAUX"]
timestamp: "2025-12-31T08:43:29Z"
published: "2022-07-04T14:02:34Z"
language: "en"
author: "bwa"
---

# Inorganic residue analysis according to ISO 19227

## 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](https://filab.fr/en/our-services/our-expertise-services/laboratory-biocompatibility-testing/laboratory-exhaustiveness-verification-iso-10993-12.md) 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](https://filab.fr/en/our-services/our-expertise-services/laboratory-biocompatibility-testing/laboratory-exhaustiveness-verification-iso-10993-12.md) 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](https://www.cofrac.fr/en)), according to validated and documented methods, helping you to comply with the requirements of the[ISO 19227](https://filab.fr/en/our-services/our-expertise-services/laboratory-biocompatibility-testing/laboratory-exhaustiveness-verification-iso-10993-12.md) standard.

## To go further

[Analysis of heavy metal residues by ICP](https://filab.fr/en/our-services/our-analysis-services/laboratory-analysis-heavy-metal.md)

[Analysis of mineral acid residues by CLI](https://filab.fr/en/our-technical-resources/laboratory-ion-chromatography.md)

[Validation of the exhaustiveness of the extraction method](https://filab.fr/en/our-services/our-expertise-services/laboratory-biocompatibility-testing/laboratory-exhaustiveness-verification-iso-10993-12.md)

[Analysis of total hydrocarbon residues (HCT) by GC-FID](https://filab.fr/en/our-services/our-expertise-services/laboratory-analyis-standard-iso-19227/analysis-of-total-hydrocarbon-residues-hct-by-gc-fid.md)

[Measurement of Total Organic Carbon (TOC) by TOC meter](https://filab.fr/en/our-services/our-expertise-services/laboratory-analyis-standard-iso-19227/laboratory-analysis-measurements-total-organic-carbon-toc.md)
