Taiwan FDA registration 5e703fb2e1efaf471cb0c2e9848227ab
“HAMAMATSU” Fluorescent Image System
TW: “濱松”螢光影像系統
Taiwan·Risk Class 2·MD·HAMAMATSU PHOTONICS K.K., JOKO FACTORY·Registered Dec 20, 2018 – Dec 20, 2028ActiveRegistration details
- Analysis ID
- 5e703fb2e1efaf471cb0c2e9848227ab
- License Form
- Ministry of Health Medical Device Import No. 031874
- Customs Code
- DHA05603187401
Company information
- Manufacturer
- HAMAMATSU PHOTONICS K.K., JOKO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- Meide Medical Devices Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1600 X-ray angiography system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 20, 2018
- Expiry Date
- Dec 20, 2028
About this record
Access comprehensive regulatory information for “HAMAMATSU” Fluorescent Image System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e703fb2e1efaf471cb0c2e9848227ab and manufactured by HAMAMATSU PHOTONICS K.K., JOKO FACTORY. The authorized representative in Taiwan is Meide Medical Devices Co., Ltd.
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