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Hager & Meisinger GmbH

Germany·DE-MF-000004966

Last updated September 17, 2026

About

Dental shop for dental practices & dental laboratories: ✓ surgical/dental instruments ✓ implant systems ✓ Manufacturers since 1888 ✓ Made in Germany

Translated from the manufacturer's own website. Source

What Hager & Meisinger GmbH makes

Hager & Meisinger GmbH manufactures surgical instrument/implant racks, including models like 31410, 31310, and 31210, as well as bone management systems for dental and surgical use. Their portfolio also includes devices such as GSRP and TSDAD, designed for dental and orthopedic applications.

The company’s products are classified as Class I and Class IIb devices and are listed in the EU’s eudamed registry. The manufacturer is based in Germany.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Hager & Meisinger GmbH primarily manufacture?

Hager & Meisinger GmbH specializes in surgical instrument and implant racks, such as models 31410, 31310, and 31210. Their portfolio also includes bone management systems, which are used in dental and surgical procedures. These devices are designed to organize, store, and manage surgical tools and implants in clinical settings.

Where is Hager & Meisinger GmbH based, and what does this imply about their regulatory environment?

Hager & Meisinger GmbH is based in Germany, which means their devices are subject to EU medical device regulations. Since their products are listed in the EU’s eudamed registry, they comply with the requirements for registration under EU Medical Device Regulation (MDR) or Medical Device Directive (MDD). This registry helps ensure transparency and traceability of devices within the European market.

Which EU regulatory database lists devices manufactured by Hager & Meisinger GmbH?

Devices from Hager & Meisinger GmbH are listed in the eudamed registry, the official EU database for medical devices. This registry is maintained under EU medical device regulations and provides public access to information about manufacturers, devices, and their regulatory status within the European Union.

How are the devices produced by Hager & Meisinger GmbH classified under EU regulations?

The devices manufactured by Hager & Meisinger GmbH fall into Class I and Class IIb categories under EU medical device regulations. Class I devices are generally considered low-risk, while Class IIb devices involve a higher level of risk and require additional conformity assessment procedures, such as clinical evaluations or designated examination bodies. The classification determines the regulatory requirements for market placement.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Germany
Address
10, Hansemannstr., Neuss, Germany
Phone
+49 2131 2012 0
PRRC Contact
Wiebke Eckhardt
EUDAMED SRN
DE-MF-000004966
FDA FEI Number
3004169071
DUNS Number
—

Catalogue (408)

Page 9 of 9
DeviceModel / ReferenceRegistriesClassStatus
Or100 Gel OR100 GEL
EUDAMED
Class IActive
Bh0012 BH0012
EUDAMED
Class IActive
Pzn13 PZN13
EUDAMEDFDA UDI
Class IActive
Bone Management 39MI206
EUDAMEDFDA UDI
Class IActive
Bone Management 39MI106
EUDAMEDFDA UDI
Class IActive
Bhwp16 BHWP16
EUDAMED
Class IActive
Bone Management 39MI202
EUDAMEDFDA UDI
Class IActive
myplant ZRA01
EUDAMEDFDA UDI
Class IActive

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