Becker GEO
- Risk class
- Class I
- CND nomenclatures code
- Y06120601
- Trade name
- Triple Action Flat Footplate Stirrup Small 1/4" offset
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 00194545171360
- Basic UDI
- 194545GEOWM
- Version date
- January 28, 2025
- Manufacturer last update
- May 07, 2021
- Active status
- No
- Manufacturer name
- Becker Orthopedic Appliance Company
- Country
- United States
- Country type
- NON_EU
- Address
- 635 Executive Drive TROY
- eguice@beckerorthopedic.net
- SRN
- IE-AR-000000592
- Country
- Ireland
- Address
- Knockmorris Co. Tipperary
- prrc@acornregulatory.com
- Telephone
- + 353 52 6176706
- Competent authority
- Health Products Regulatory Authority, Medical Devices Department
- 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
PASSIVE ANKLE-FOOT ORTHOSES
Access comprehensive regulatory information for Becker GEO 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 00194545171360 and manufactured by Becker Orthopedic Appliance Company in United States.
This page provides complete registration details including trade name (Triple Action Flat Footplate Stirrup Small 1/4" offset), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), 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.