Taiwan FDA registration c03f7b19778e2ef3024588457d09b876
WAN DER EXTREMITY ORTHOSIS (NON-STERILE)
TW: 萬德肢體矯正護具（未滅菌）
Taiwan·Risk Class 1·MD·Wande Disabled Equipment Co., Ltd. Zhonghe Factory·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- c03f7b19778e2ef3024588457d09b876
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 000206
- Customs Code
- DHY08300020606
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WAN DER DIABLED PERSON'S AID & SUPPLIES. CO., LTD.
Product details
- Intended Use
- Medical equipment worn on the upper or lower limbs to support, correct, prevent deformation or straighten the body structure for functional improvement.
- 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, 2025
About this record
Access comprehensive regulatory information for WAN DER EXTREMITY 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 c03f7b19778e2ef3024588457d09b876 and manufactured by Wande Disabled Equipment Co., Ltd. Zhonghe Factory. The authorized representative in Taiwan is WAN DER DIABLED PERSON'S AID & SUPPLIES. CO., LTD..
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