Taiwan FDA registration 787628b670760741a1f4e71be747b3be
"Chongwei" Truncal orthosis (Non-Sterile)
TW: "重維"軀幹裝具 (未滅菌)
Taiwan·Risk Class 1·MD·Heavy Maintenance Rehabilitation Products Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 787628b670760741a1f4e71be747b3be
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 003395
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Heavy Maintenance Rehabilitation Products Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3490 Torso Gear
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Chongwei" Truncal orthosis (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 787628b670760741a1f4e71be747b3be and manufactured by Heavy Maintenance Rehabilitation Products Co., Ltd. The authorized representative in Taiwan is Heavy Maintenance Rehabilitation Products Co., Ltd.
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