MD Atlas update: Jun 10, 2026

GD Dentaltechnik GmbH

DE-PR-000056015

System / procedure pack producerActive

Address: Karl-Hermann-Flach-Str., 15a 61440 Oberursel
Role: System / procedure pack producer
Date of registration: Jun 8, 2026
Country: Germany

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GD Dentaltechnik GmbH is a system and procedure pack producer registered in EUDAMED. Headquartered in Oberursel, Germany. Explore the regulatory profile, devices and certificates on MD Atlas.

Role
Country
Date of registration
Address

MD Atlas update: Jun 10, 2026

GD Dentaltechnik GmbH

DE-PR-000056015

System / procedure pack producerActive

Address: Karl-Hermann-Flach-Str., 15a 61440 Oberursel
Role: System / procedure pack producer
Date of registration: Jun 8, 2026
Country: Germany

Is this your company? Claim it to add your logo, story and links — free.Claim this page

GD Dentaltechnik GmbH is a system and procedure pack producer registered in EUDAMED. Headquartered in Oberursel, Germany. Explore the regulatory profile, devices and certificates on MD Atlas.

About GD Dentaltechnik GmbH

SRN An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor. View in glossary →: DE-PR-000056015
Role: System / procedure pack producer
Country: Germany
Organization name: GD Dentaltechnik GmbH
EU VAT number: DE308109110
EORI: DE235923147254386
Trade register: HRB16251
Date of registration: Jun 8, 2026

Contact details for GD Dentaltechnik GmbH

Phone: +496171951760
Email: info@gd-dental.de
Website: www.gd-dental.de
Address: 15A, KARL-HERMANN-FLACH-STR. 61440 OBERURSEL GERMANY

Competent authority

Name: DE/CA23 - Regierungspräsidium Darmstadt Dezernat IV/Da 45.2
SRN An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor. View in glossary →: DE-CA-040
Phone: +49 (6151) 12 4001
Email: arbeitsschutz@rpda.hessen.de

Role and obligations in EUDAMED

A producer of systems or procedure packs combines CE-marked devices to place a system or procedure pack on the market under the conditions of Article 22 of the MDR (2017/745).