Taiwan FDA registration 70ca0b999897603e3a729e77fa9e7684
"Herdegen France" Flotation Cushion (Non-Sterile)
TW: "法國荷迪根" 浮動坐墊 (未滅菌)
Taiwan·Risk Class 1·MD·HERDEGEN SAS·Registered May 23, 2019 – May 23, 2024ExpiredRegistration details
- Analysis ID
- 70ca0b999897603e3a729e77fa9e7684
- License Form
- Ministry of Health Medical Device Import No. 020478
- Customs Code
- DHA09402047802
Company information
- Manufacturer
- HERDEGEN SAS
- Manufacturer Country
- France
- Authorized Representative
- MEDEPOT CO., LTD
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3175 floating seat cushion
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 23, 2019
- Expiry Date
- May 23, 2024
About this record
Access comprehensive regulatory information for "Herdegen France" Flotation Cushion (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 70ca0b999897603e3a729e77fa9e7684 and manufactured by HERDEGEN SAS. The authorized representative in Taiwan is MEDEPOT CO., LTD.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices