Taiwan FDA registration edd13fadc7ad13e5b05483453cb83669
“KUAI YI PAO”Lycra Limb Orthosis (Non-Sterile)
TW: “快意寶”萊卡護具 (未滅菌)
Taiwan·Risk Class 1·MD·Aimin Eisai Co., Ltd. Plant 2·Registered Oct 01, 2021 – Oct 31, 2022CancelledRegistration details
- Analysis ID
- edd13fadc7ad13e5b05483453cb83669
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 001902
Company information
- Manufacturer
- Aimin Eisai Co., Ltd. Plant 2
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Aimin Eisai Co., Ltd. Plant 2
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
- Cancellation Date
- Oct 28, 2022
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業;;未展延而逾期者
About this record
Access comprehensive regulatory information for “KUAI YI PAO”Lycra 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 edd13fadc7ad13e5b05483453cb83669 and manufactured by Aimin Eisai Co., Ltd. Plant 2. The authorized representative in Taiwan is Aimin Eisai Co., Ltd. Plant 2.
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