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IFU Protected Content

Electronic Instructions for Use

Electronic Instructions for Use are provided in standard adobe acrobat pdf format.

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Ankyras IFU

Name
eVersion
Regulatory
Language
Creation
Ankyras
Regulated
Latest
4.0
Investigational
Spanish
Ankyras
Regulated
4.0
Investigational
Spanish
Ankyras
Regulated
Latest
4.0
CE
Spanish
Ankyras
Regulated
4.0
CE
Spanish
Ankyras
Regulated
Latest
4.0
Investigational
English
Ankyras
Regulated
4.0
Investigational
English
Ankyras
Regulated
Latest
4.0
CE
English
Ankyras
Regulated
4.0
CE
English
Ankyras 3.0 FDA EN
Regulated
Latest
3.0
FDA
English
Ankyras 3.0 FDA EN
Regulated
3.0
FDA
English
To access previous versions of the Ankyras IFU, please visit the Galgo Medical website.  
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Disclaimer & Regulatory Information

Ankyras is manufactured by Mentice Spain S.L. and distributed by Mentice subsidiaries and partners in approved markets.


Mentice Spain SL: Mentice Spain SL has obtained the ISO 13485 certification with number MD 784027
Ankyras certifications: The Ankyras product complies with the Medical Device Regulation (EU CE Mark, MDR 784032) and the UK Conformity Assessed (UKCA 784033)