Taiwan FDA registration f50c3dacd93e813eb7e94b9766d52467
KEN DALL Limb orthosis (Non-sterile)
TW: 肯達路 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·Kenda Road Enterprise Co., Ltd. Xinzhuang Factory·Registered Jun 13, 2023 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- f50c3dacd93e813eb7e94b9766d52467
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. a00255
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Kenda Road Enterprise Co., Ltd. Xinzhuang Factory
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O3475 Body Equipment
Dates and status
- Registration Date
- Jun 13, 2023
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for KEN DALL 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 f50c3dacd93e813eb7e94b9766d52467 and manufactured by Kenda Road Enterprise Co., Ltd. Xinzhuang Factory. The authorized representative in Taiwan is Kenda Road Enterprise Co., Ltd. Xinzhuang Factory.
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