Taiwan FDA registration 1df09fc2e77df4af95f47b71dac258aa
"BONEMETAL" Truncal orthosis (Non-Sterile)
TW: "溋溢" 軀幹裝具 (未滅菌)
Taiwan·Risk Class 1·MD·BONE METAL CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 1df09fc2e77df4af95f47b71dac258aa
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 006102
Company information
- Manufacturer
- BONE METAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BONE METAL 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 "BONEMETAL" 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 1df09fc2e77df4af95f47b71dac258aa and manufactured by BONE METAL CO., LTD.. The authorized representative in Taiwan is BONE METAL CO., LTD..
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