Taiwan FDA registration 026323958a3a121dd7b60a9e41cdca63
"ALLARD" Limb Orthosis (Non-Sterile)
TW: "艾拉德" 肢體裝具 (未滅菌)
Registration details
- Analysis ID
- 026323958a3a121dd7b60a9e41cdca63
- License Form
- Ministry of Health Medical Device Import No. 013746
- Customs Code
- DHA09401374607
Company information
- Manufacturer
- ALLARD USA INC.
- Manufacturer Country
- United States
- Authorized Representative
- CHENG CHUAN P&O 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 03, 2014
- Expiry Date
- Jan 03, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "ALLARD" 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 026323958a3a121dd7b60a9e41cdca63 and manufactured by ALLARD USA INC.. The authorized representative in Taiwan is CHENG CHUAN P&O CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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