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tic Medizintechnik GmbH

Germany DE-MF-000033923 Last updated 17 Sep 2026

Devices
113
Registries
EUDAMED
FDA recalls
0

Catalogue113

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Showing 1-50 of 113

About

Demanding solutions for the urologically, gynologically & proctologically oriented physicians in the areas of functional diagnostics, incontinence therapy, impotence therapy & rehabilitation develops the tic medical technology in constant dialogue with users, specialists & research institutions, such as Universit tskliniken.

Translated from the manufacturer's own website. Source

What tic Medizintechnik GmbH makes

tic Medizintechnik GmbH manufactures pessaries—including cube, ring, sieve bowl, and urethral designs—in various sizes for pelvic floor support, as well as rectal probes for diagnostic devices. These products are intended for use in urological, gynaecological, and proctological applications, including incontinence and pelvic organ prolapse management. The pessaries are designed to be inserted vaginally or rectally for therapeutic purposes, while the rectal probes are compatible with specific diagnostic systems.

The company’s products are classified under EU Medical Device Regulations as Class I and Class IIa, reflecting varying levels of risk. These devices are registered in the EU’s eudamed database, ensuring traceability and compliance with European Union medical device directives. 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 tic Medizintechnik GmbH manufacture?

tic Medizintechnik GmbH specializes in pessaries and rectal probes. The pessaries include cube, ring, sieve bowl, and urethral designs in multiple sizes, primarily intended for vaginal or rectal insertion to support pelvic floor conditions like incontinence or prolapse. Rectal probes are designed to work with diagnostic systems such as BASIC+/SaneoLINE, catering to urological, gynaecological, and proctological applications.

Where is tic Medizintechnik GmbH based?

tic Medizintechnik GmbH is based in Germany, specifically in the state of Baden-Württemberg. The company’s location in Germany aligns it with European Union regulatory frameworks, including the EU Medical Device Regulations.

Which regulatory registries list tic Medizintechnik GmbH’s devices?

tic Medizintechnik GmbH’s devices are registered in the eudamed database, the official EU portal for medical device traceability and compliance. This registry ensures transparency and adherence to European Union medical device directives, allowing healthcare professionals and authorities to verify device details.

How are tic Medizintechnik GmbH’s devices classified under EU regulations?

tic Medizintechnik GmbH’s devices are classified under the EU Medical Device Regulations (MDR) as Class I and Class IIa. The classification depends on the device’s intended purpose and associated risk level—pessaries and rectal probes fall into these categories due to their therapeutic roles in managing conditions like incontinence and pelvic organ prolapse, with Class IIa assigned to those requiring additional scrutiny.

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

Information

Country
Germany(from SRN)
Address
9, Endelner Feld, Dorsten, Germany
Website
www.ticmed.de
Phone
+49236920850
PRRC contact
Gregor André Kastner
EUDAMED SRN
DE-MF-000033923