HandTutor
- Risk class
- Class I
- CND nomenclatures code
- Z120602
- Trade name
- HandTutor
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 05065016488032
- Basic UDI
- 5065016488HandtutorLU
- Version date
- July 10, 2023
- Manufacturer last update
- May 16, 2023
- Active status
- Yes
- Manufacturer name
- TMA MEDICAL EQUIPMENT LTD
- Country
- United Kingdom (ex Northern Ireland)
- Country type
- NON_EU
- Address
- 177 Ashfield Avenue, Bushey
- tmamedical.uk@gmail.com
- SRN
- DK-AR-000017664
- Country
- Denmark
- Address
- 52 2 th Blokland Albertslund
- info@techstandi.com
- Telephone
- 08000016832
- Competent authority
- Danish Medicines Agency, Pharmacovigilance & Medical Devices
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Poland
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Turkey:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
PHYSIOTHERAPY EQUIPMENT
Access comprehensive regulatory information for HandTutor in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05065016488032 and manufactured by TMA MEDICAL EQUIPMENT LTD in United Kingdom (ex Northern Ireland).
This page provides complete registration details including trade name (HandTutor), manufacturer information, authorized representative details, competent authority (Danish Medicines Agency, Pharmacovigilance & Medical Devices), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.