Taiwan FDA registration 74b1bbd3298cdf75060129dbff425ab0
Orliman Limb orthosis (Non-sterile)
TW: 歐立盟 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·ORLIMAN·Registered Jun 18, 2022 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 74b1bbd3298cdf75060129dbff425ab0
- License Form
- Ministry of Health Medical Device Import Registration No. a00075
- Customs Code
- DHA084a0007502
Company information
- Manufacturer
- ORLIMAN
- Manufacturer Country
- Spain
- Authorized Representative
- LIESIEN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O3475 Body Equipment
Dates and status
- Registration Date
- Jun 18, 2022
- Expiry Date
- Oct 31, 2023
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 74b1bbd3298cdf75060129dbff425ab0 and manufactured by ORLIMAN. The authorized representative in Taiwan is LIESIEN ENTERPRISE CO., LTD..
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