Disposable Guide Wire
- Risk class
- Class IIa
- CND nomenclatures code
- G0399
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06959664954942
- Basic UDI
- 695966495041000013S
- Version date
- June 04, 2024
- Manufacturer last update
- June 04, 2024
- Active status
- No
- Manufacturer name
- Hangzhou AGS MedTech Co.,Ltd.
- Country
- China
- Country type
- NON_EU
- Address
- No.389 Building 2, 5 and 7, Xingzhong Road, Linping District, Hangzhou, Zhejiang
- wangsf@bioags.com
- SRN
- DE-AR-000000001
- Country
- Germany
- Address
- 80 Eiffestraße Hamburg
- shholding@hotmail.com
- Telephone
- +49 40 2513175
- Competent authority
- DE/CA05 - Behorde fur Justiz und Verbraucherschutz
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- France
- 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
DIGESTIVE ENDOSCOPY DEVICES - OTHER
Access comprehensive regulatory information for Disposable Guide Wire 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 06959664954942 and manufactured by Hangzhou AGS MedTech Co.,Ltd. in China.
This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA05 - Behorde fur Justiz und Verbraucherschutz), 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.