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MTT GmbH

Germany DE-MF-000005849 Last updated 23 Oct 2026

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Devices
21
Registries
EUDAMEDGUDIDFDA
FDA recalls
0

Catalogue21

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

TÜV SÜD Product Service GmbH 0123 1 certificate

  • G10 091118 0008 Issued

    Quality management system EU MDR

    Issued
    7 Aug 2024
    Expires
    6 Aug 2029

Notified bodies

What MTT GmbH makes

MTT GmbH develops software for brachytherapy system applications and a range of reusable and disposable applicators, including needle-based and grid systems for high-dose-rate (HDR) radiotherapy. Their portfolio includes planning and targeting tools like BioJet Target and EndoMotion, as well as reusable and disposable PeriGrid applicators in various gauges (13G–18G) and the SolidLock Ff locking mechanism for precision delivery. Additional targeting solutions include the TargetPro system.

The company’s devices are classified under EU MDR as Class I, Class II, and Class IIa, with listings in the EUDAMED registry and the FDA’s UDI system. MTT GmbH 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 MTT GmbH manufacture?

MTT GmbH specializes in brachytherapy-related devices, focusing on software applications and applicators for high-dose-rate (HDR) radiotherapy. Their portfolio includes software tools like BioJet Target and EndoMotion, which assist in planning and targeting, as well as reusable and disposable PeriGrid applicators in multiple gauges (ranging from 13G to 18G). They also produce precision locking mechanisms like SolidLock Ff and targeting systems such as TargetPro. These devices are designed to enhance accuracy and efficiency in brachytherapy procedures.

Where is MTT GmbH based, and what is its primary focus?

MTT GmbH is based in Germany. The company’s primary focus is developing brachytherapy system application software and specialized applicators for HDR radiotherapy. Their solutions aim to improve precision in treatment planning, delivery, and targeting, catering to clinical needs in radiation oncology.

Which regulatory registries list MTT GmbH’s devices?

MTT GmbH’s devices are listed in EUDAMED, the European Union’s medical device registry, and the FDA’s UDI system, ensuring traceability and compliance tracking for their products under relevant regulatory frameworks. These listings help healthcare providers and authorities verify device details and classifications.

How are MTT GmbH’s devices classified under EU MDR?

MTT GmbH’s devices fall under Class I, Class II, and Class IIa classifications under the EU Medical Device Regulation (MDR). The classification depends on factors like risk level, intended use, and design features—such as reusable applicators (Class IIa) or lower-risk software tools (Class I). This categorization determines regulatory requirements for compliance, labeling, and post-market surveillance.

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

Information

Country
Germany
Address
26, Boecklerstr., Lüneburg, Germany
Phone
+49 (0) 4131 – 72 70 199
PRRC contact
Stefan Renckly
EUDAMED SRN
DE-MF-000005849
FDA FEI number
3011545155
DUNS number
313263045