Taiwan FDA registration a551206da9014718f6e9a86c41ee25d1
"OPED Asia-Pacific" Limb orthosis（Non-Sterile）
TW: "歐霈德亞太" 肢體裝具（未滅菌）
Taiwan·Risk Class 1·MD·ARROW MEDICAL LTD·Registered Nov 24, 2015 – Nov 24, 2020CancelledRegistration details
- Analysis ID
- a551206da9014718f6e9a86c41ee25d1
- License Form
- Ministry of Health Medical Device Import No. 015892
- Customs Code
- DHA09401589202
Company information
- Manufacturer
- ARROW MEDICAL LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- OPED ASIA-PACIFIC COMPANY LIMITED
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
- Nov 24, 2015
- Expiry Date
- Nov 24, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "OPED Asia-Pacific" 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 a551206da9014718f6e9a86c41ee25d1 and manufactured by ARROW MEDICAL LTD. The authorized representative in Taiwan is OPED ASIA-PACIFIC COMPANY LIMITED.
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