Taiwan FDA registration 87fbc22ac9385993c2465e4863e4f1bf
“Medikit” Supercath C-Pro
TW: “美迪克”安全血液透析血管留置針
Taiwan·Risk Class 2·MD·TOGO MEDIKIT CO., LTD. HYUGA FACTORY·Registered May 24, 2019 – May 24, 2024ExpiredRegistration details
- Analysis ID
- 87fbc22ac9385993c2465e4863e4f1bf
- License Form
- Ministry of Health Medical Device Import No. 032673
- Customs Code
- DHA05603267306
Company information
- Manufacturer
- TOGO MEDIKIT CO., LTD. HYUGA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- EVERMEDICAL COMPANY LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5540 Blood access devices and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 24, 2019
- Expiry Date
- May 24, 2024
About this record
Access comprehensive regulatory information for “Medikit” Supercath C-Pro in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 87fbc22ac9385993c2465e4863e4f1bf and manufactured by TOGO MEDIKIT CO., LTD. HYUGA FACTORY. The authorized representative in Taiwan is EVERMEDICAL COMPANY LTD..
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