Walking Frame
- Risk class
- Class I
- CND nomenclatures code
- Y120606
- Trade name
- Extra Large wheeled frame
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 05052893002604
- Basic UDI
- 5052893WAFEX
- Version date
- March 05, 2024
- Manufacturer last update
- March 20, 2024
- Active status
- No
- Manufacturer name
- Trulife Ltd
- Country
- United Kingdom (ex Northern Ireland)
- Country type
- NON_EU
- Address
- 41 Amos Road Sheffield
- demsden@trulife.com
- Name
- MDSS GmbH
- SRN
- DE-AR-000005430
- Country
- Germany
- Address
- 41 Schiffgraben Hannover
- info@mdssar.com
- Competent authority
- DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Ireland
- 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, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
WHEELED WALKER
Access comprehensive regulatory information for Walking Frame 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 05052893002604 and manufactured by Trulife Ltd in United Kingdom (ex Northern Ireland).
This page provides complete registration details including trade name (Extra Large wheeled frame), manufacturer information, authorized representative details, competent authority (DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover), 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.