EUDAMED registration D-4603990Z3YesEGI External Power Supply 100 (Finished)
- Risk class
- Class IIa
- CND nomenclatures code
- Z12100303
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- D-4603990Z3
- Basic UDI
- B-4603990Z3
- Version date
- July 14, 2022
- Manufacturer last update
- January 11, 2023
- Active status
- Yes
- Manufacturer name
- Magstim Inc.
- Country
- United States
- Country type
- NON_EU
- Address
- 78 Centennial Loop Eugene
- regulatory@magstim.com
- SRN
- DE-AR-000005009
- Country
- Germany
- Address
- 20 Borngasse Braunfels
- g.froemel@mps-gmbh.eu
- Telephone
- +49 6442962073
- Competent authority
- DE/CA36 - Regierungspräsidium Gießen Abteilung II_Dezernat 25.1 - Arbeitsschutz Gießen I
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Germany
- Market available
- Austria:2017-03-03~2024-05-26, Belgium:2017-03-03~2024-05-26, Bulgaria:2017-03-03~2024-05-26, Croatia:2017-03-03~2024-05-26, Cyprus:2017-03-03~2024-05-26, Czechia:2017-03-03~2024-05-26, Denmark:2017-03-03~2024-05-26, Estonia:2017-03-03~2024-05-26, Finland:2017-03-03~2024-05-26, France:2017-03-03~2024-05-26, Germany:2017-03-03~2024-05-26, Greece:2017-03-03~2024-05-26, Hungary:2017-03-03~2024-05-26, Iceland:2017-03-03~2024-05-26, Ireland:2017-03-03~2024-05-26, Italy:2017-03-03~2024-05-26, Latvia:2017-03-03~2024-05-26, Liechtenstein:2017-03-03~2024-05-26, Lithuania:2017-03-03~2024-05-26, Luxembourg:2017-03-03~2024-05-26, Malta:2017-03-03~2024-05-26, Netherlands:2017-03-03~2024-05-26, Norway:2017-03-03~2024-05-26, Poland:2017-03-03~2024-05-26, Portugal:2017-03-03~2024-05-26, Romania:2017-03-03~2024-05-26, Slovakia:2017-03-03~2024-05-26, Slovenia:2017-03-03~2024-05-26, Spain:2017-03-03~2024-05-26, Sweden:2017-03-03~2024-05-26, Turkey:2017-03-03~2024-05-26, United Kingdom (Northern Ireland only):2017-03-03~2024-05-26
- Human tissues
- No
- Animal tissues
- No
SYSTEMS FOR ANALYSING AND MANAGING EEG TRACES
Access comprehensive regulatory information for EGI External Power Supply 100 (Finished) in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI D-4603990Z3 and manufactured by Magstim Inc. in United States.
This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA36 - Regierungspräsidium Gießen Abteilung II_Dezernat 25.1 - Arbeitsschutz Gießen I), 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.