Connection System Cables
- Risk class
- Class I
- CND nomenclatures code
- N010180
- Trade name
- Lightweight CABRIO Cable
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 00841823106506
- Basic UDI
- 08418231RA6aJS
- Version date
- November 18, 2024
- Manufacturer last update
- September 09, 2024
- Active status
- No
- Manufacturer name
- Ad-Tech Medical Instrument Corp.
- Country
- United States
- Country type
- NON_EU
- Address
- 400 West Oakview Parkway Oak Creek
- regulatory@adtechmedical.com
- Name
- E C REP LIMITED
- SRN
- IE-AR-000003995
- Country
- Ireland
- Address
- 5 Fitzwilliam Square East Dublin D2
- info@ecrep.ie
- Telephone
- +353 89 225 1951
- 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
NEUROPHYSIOLOGY DEVICES - ACCESSORIES
Access comprehensive regulatory information for Connection System Cables 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 00841823106506 and manufactured by Ad-Tech Medical Instrument Corp. in United States.
This page provides complete registration details including trade name (Lightweight CABRIO Cable), 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.