MTT GmbH
Germany DE-MF-000005849 Last updated 23 Oct 2026
Is this your brand? Sign in to claim this brand
- Devices
- 21
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
BioJet Target 3 Ref 3
EndoMotion Ref HW-001-015
PeriGrid HDR 16G Ref HW-005-027
PeriGrid HDR 14G Ref HW-005-033
PeriGrid Reusable 14G Ref HW-005-012
PeriGrid Reusable 15G Ref HW-005-008
SolidLock F Ref HW-001-013
PeriGrid Reusable 17G Ref HW-005-004
PeriGrid Reusable 16G Ref HW-005-006
PeriGrid Reusable 13G Ref HW-005-014
PeriGrid Disposable 18G Ref HW-005-001
SolidLock Ff Ref HW-001-014
TargetPro Ref HW-005-037
PeriGrid HDR 18G Ref HW-005-019
SolidLock F-500ext Ref HW-001-027
PeriGrid HDR 17G Ref HW-005-022
SolidLock HS-500ext Ref HW-001-011
PeriGrid Reusable 18G Ref HW-005-002
PeriGrid HDR 17G Special 0.33 Ref HW-005-025
PeriGrid HDR 15G Ref HW-005-030
Solid Lock HS Ref HW-001-010
EUDAMED certificates
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
Related companies
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.
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.
Information
- Country
- Germany
- Address
- 26, Boecklerstr., Lüneburg, Germany
- Website
- www.medical-tt.com
- [email protected]
- Phone
- +49 (0) 4131 – 72 70 199
- PRRC contact
- Stefan Renckly
- EUDAMED SRN
- DE-MF-000005849
- FDA FEI number
- 3011545155
- DUNS number
- 313263045