Taiwan FDA registration 149afb05bfbed48cb061a48ce4b04f2e
"Orliman" Limb orthosis (Non-Sterile)
TW: "歐立盟" 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·ORLIMAN·Registered Jan 15, 2016 – Jan 15, 2021CancelledRegistration details
- Analysis ID
- 149afb05bfbed48cb061a48ce4b04f2e
- License Form
- Ministry of Health Medical Device Import No. 016080
- Customs Code
- DHA09401608007
Company information
- Manufacturer
- ORLIMAN
- Manufacturer Country
- Spain
- Authorized Representative
- LIESIEN ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 15, 2016
- Expiry Date
- Jan 15, 2021
- Cancellation Date
- Aug 04, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Orliman" Limb 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 149afb05bfbed48cb061a48ce4b04f2e and manufactured by ORLIMAN. The authorized representative in Taiwan is LIESIEN ENTERPRISE CO., LTD..
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