Manual hospital bed
- Risk class
- Class I
- CND nomenclatures code
- V080602
- Trade name
- FUGONG Manual hospital bed
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06975736670060
- Basic UDI
- 697573667SDCXX
- Version date
- November 22, 2022
- Manufacturer last update
- November 04, 2022
- Active status
- No
- Manufacturer name
- Hebei Fuda Metal Working Medical Equipment Co., Ltd.
- Country
- China
- Country type
- NON_EU
- Address
- Fentai Village, Ansu Town, Xushui District Baoding City, Hebei Province
- 454424705@qq.com
- SRN
- NL-AR-000002066
- Country
- Netherlands
- Address
- 36 Zonnehof Nootdorp
- office@kingsmead-service.com
- Telephone
- +31(0) 64 6571 005
- Competent authority
- Ministerie van Volksgezondheid, Welzijn en Sport
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Austria
- Market available
- Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece: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, United Kingdom (Northern Ireland only):None~None, Austria:None~None
- Human tissues
- No
- Animal tissues
- No
MANUAL MEDICAL BEDS
Access comprehensive regulatory information for Manual hospital bed 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 06975736670060 and manufactured by Hebei Fuda Metal Working Medical Equipment Co., Ltd. in China.
This page provides complete registration details including trade name (FUGONG Manual hospital bed), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.