TRUEinvivo Limited
United Kingdom (ex Northern Ireland) UK-MF-000036202 Last updated 22 Oct 2026
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- Devices
- 4
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
DOSEmapper 3D Ref DM3D
DOSEmapper 1D Ref DM1D
DOSEmapper 2D Ref DM2D
DOSEmapper Beads Ref DM0L
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About
Why DOSEmappers™? Linear DOSEmappers™ on a gloved hand Up to 30% of radiotherapy patients experience harmful side effects requiring extra treatments and costs, sometimes for life. DOSEmappers™ enable adaptive personalised radiotherapy for better and safer outcomes
What TRUEinvivo Limited makes
TRUEinvivo Limited manufactures a range of DOSEmapper devices, including 1D, 2D, and 3D versions, as well as DOSEmapper Beads. These tools are designed to support adaptive radiotherapy planning by mapping dose distributions in real-time, aiding precision treatment for patients.
The DOSEmapper portfolio is classified under Class I medical devices and is registered in the EU’s eudamed database. TRUEinvivo Limited is based in the United Kingdom.
Frequently asked questions
What types of medical devices does TRUEinvivo Limited manufacture?
TRUEinvivo Limited specialises in a range of DOSEmapper devices, including linear (1D), planar (2D), volumetric (3D) versions, and DOSEmapper Beads. These tools are designed to help map radiation dose distributions in real-time, supporting more precise and adaptive radiotherapy planning for patients.
Where is TRUEinvivo Limited based?
TRUEinvivo Limited is headquartered in the United Kingdom. The company’s location in the UK aligns with its focus on developing innovative medical technologies for global use, particularly in radiotherapy.
Are TRUEinvivo Limited’s devices listed in any regulatory registries?
Yes, TRUEinvivo Limited’s DOSEmapper devices are registered in the EU’s eudamed database. This registry is used to track medical devices authorised for use within the European Economic Area, ensuring transparency and traceability.
How are TRUEinvivo Limited’s devices classified under medical device regulations?
TRUEinvivo Limited’s DOSEmapper devices fall under Class I classification. This classification is typically assigned to low-risk devices that pose minimal risk to patients, though individual devices must still meet regulatory requirements for safety and performance before authorisation.
Information
- Country
- United Kingdom (ex Northern Ireland)
- Address
- 1, Hampshire Terrace, Portsmouth, United Kingdom (ex Northern Ireland)
- Website
- www.trueinvivo.co.uk
- [email protected]
- Phone
- +44 2392 004495
- PRRC contact
- Mike Stroud
- EUDAMED SRN
- UK-MF-000036202