Publisher:
Global D SASU, with capital of €1,116,536, located at 118 Avenue Marcel Mérieux ZI de Sacuny 69530 Brignais France, registered with the Lyon B Trade and Companies Register under number 752 283 739
Telephone number: +33 (0)4 78 56 97 00 Email: contact@globald.com
Developer:
Harvest Agency SRL, with capital of €101,000, located at 21 RUE D’ALGERIE IMM SAINTE MARIE DES TERREAUX 21-23, 69001 LYON France, registered with the Lyon B Trade and Companies Register under number 504838012
Host:
WP SERVEUR SAS, with capital of €600, located at 20 RUE ALBERT EINSTEIN, 77420 CHAMPS-SUR-MARNE France, registered with the Meaux Trade and Companies Register under number 808840474
Publishing Director:
Mr. Benoit RODRIGUEZ DE SOUZA – contact@globald.com
Communications Director:
Mr. Régis PROVIGNON – communication@globald.com
Hyperlinks:
Global D does not control websites linked to its own and therefore cannot be held responsible for their content. Users are solely responsible for any risks associated with using these websites. They must comply with their terms of use.
Products:
- Dental implant system (In‑Kone®, twinKon® and EVL® ranges): The products presented are Class I, IIa and IIb Medical Devices bearing the CE mark and intended for healthcare professionals in dental implantology. They are used to replace missing teeth.
- Cranio-maxillofacial and pre-implant osteosynthesis system (ORTRAUTEK, MINITEK/MICROTEK, CARCITEK and GRAFTEK ranges): The products presented are Class I, IIa and IIb Medical Devices bearing the CE mark, intended for healthcare professionals in Cranio-Maxillofacial and Pre-implant Surgery. They are used for cranio-maxillofacial bone stabilisation and fixation during osteosynthesis and the bone consolidation period. In France, cranio-maxillofacial implants are subject to the Social Security reimbursement scheme. Medical devices dedicated to pre-implant surgery are not subject to the Social Security reimbursement scheme.
- Orthodontic osteosynthesis system (ANCOTEK range): The products presented are Class I, IIa and IIb Medical Devices bearing the CE mark and intended for use by healthcare professionals in orthodontics. They are used for fixation to the jaw during orthodontic treatment, with the aim of restoring the correct position of the teeth and bone bases in cases of malocclusion.
Please consult the instructions for use before use.
The instructions for use are available in digital format. A QR code and URL link are provided on the device label. Paper instructions are also available on request at the following address: quality@globald.com at no additional cost within 7 days.
All devices are available for export subject to obtaining the approvals in force in the countries concerned. If in doubt or for further information, please contact us.