Taiwan FDA registration a9340aae78681e7fbb0d6d5222203876
"WAN DER" SPINAL ORTHOSIS (NON-STERILE)
TW: "萬德" 脊椎矯正裝具(未滅菌)
Registration details
- Analysis ID
- a9340aae78681e7fbb0d6d5222203876
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 000171
- Customs Code
- DHY08300017100
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 used to support or immobilize fractures, injuries with excessive force or sprains to the trunk and neck.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3490 Torso Gear
- 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" SPINAL 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 a9340aae78681e7fbb0d6d5222203876 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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