Geister Medizin Technik GmbH
US Last updated 23 May 2026
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- Devices
- 1,673
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Showing 1-50 of 1,673
FDA establishments
- Geister Medizintechnik GmbH TUTTLINGEN Baden-Wurttemberg · DE FEI 3004053982
What Geister Medizin Technik GmbH makes
Geister Medizin Technik GmbH manufactures reusable surgical instruments including vascular dilators, vascular clamps, surgical soft-tissue manipulation forceps, surgical bulldog clamps, general-purpose surgical scissors, suturing needle holders, hand-held retractors, and surgical retraction system mounting frames.
The company's portfolio includes Class I and Class II devices listed in the FDA UDI registry, and they are based in the US.
Frequently asked questions
What does Geister Medizin Technik GmbH manufacture?
Geister Medizin Technik GmbH manufactures reusable surgical instruments including vascular dilators, vascular clamps, surgical soft-tissue manipulation forceps, surgical bulldog clamps, general-purpose surgical scissors, suturing needle holders, hand-held retractors, and surgical retraction system mounting frames.
Where is Geister Medizin Technik GmbH based?
Geister Medizin Technik GmbH is based in the United States, as indicated by the country designation in the device data.
Which regulatory registries list Geister Medizin Technik GmbH's devices?
The company's devices are listed in the FDA UDI registry, which tracks unique device identifiers for medical devices marketed in the United States.
How are Geister Medizin Technik GmbH's devices classified?
The company's devices are classified as Class I and Class II, which are regulatory categories indicating the level of control necessary to assure safety and effectiveness, with Class II devices requiring special controls.
Information
- Country
- US