Taiwan FDA registration ddb220d1bc3f02384971becc7a30c175
"HandyRehab" Continuous Passive Motion Device (Non-sterile)
TW: "韓迪瑞賀博" 連續式被動關節活動器 (未滅菌)
Taiwan·Risk Class 1·MD·ZUNOSAKI LIMITED.·Registered Jan 28, 2021 – Jan 28, 2026ExpiredRegistration details
- Analysis ID
- ddb220d1bc3f02384971becc7a30c175
- License Form
- Ministry of Health Medical Device Import No. 022276
- Customs Code
- DHA09402227600
Company information
- Manufacturer
- ZUNOSAKI LIMITED.
- Manufacturer Country
- Hong Kong
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Continuous Passive Joint Activator (O.0006)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O0006 Continuous Passive Joint Activator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 28, 2021
- Expiry Date
- Jan 28, 2026
About this record
Access comprehensive regulatory information for "HandyRehab" Continuous Passive Motion Device (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 ddb220d1bc3f02384971becc7a30c175 and manufactured by ZUNOSAKI LIMITED.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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