Taiwan FDA registration b07721d16243a3a5eeb18fb6d28b027a
"Renfu" Patient Fixation in Radiation Oncology (Non-Sterile)
TW: "仁福" 放射線造影固定裝置 (未滅菌)
Taiwan·Risk Class 1·MD·GUANGZHOU RENFU MEDICAL EQUIPMENT CO., LTD·Registered Oct 01, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- b07721d16243a3a5eeb18fb6d28b027a
- License Form
- Ministry of Health Medical Device Land Transport Registration No. 003459
- Customs Code
- DHA08600345905
Company information
- Manufacturer
- GUANGZHOU RENFU MEDICAL EQUIPMENT CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- INTERMEDIC INC.
Product details
- Intended Use
- Limited to the first level recognition range of radiographic head fixator (P.1920) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1920 Radiographic head holder
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for "Renfu" Patient Fixation in Radiation Oncology (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 b07721d16243a3a5eeb18fb6d28b027a and manufactured by GUANGZHOU RENFU MEDICAL EQUIPMENT CO., LTD. The authorized representative in Taiwan is INTERMEDIC INC..
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