Taiwan FDA registration ed3901c73e0d1b5d46914d14ef4602f2
“Wiltrom” Vertebral Body Augmentation System
TW: “威創”可擴張椎體強化系統
Taiwan·Risk Class 2·MD·Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory·Registered Mar 18, 2019 – Dec 08, 2028ActiveRegistration details
- Analysis ID
- ed3901c73e0d1b5d46914d14ef4602f2
- License Form
- Ministry of Health Medical Device Manufacturing No. 006324
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WILTROM CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 18, 2019
- Expiry Date
- Dec 08, 2028
About this record
Access comprehensive regulatory information for “Wiltrom” Vertebral Body Augmentation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed3901c73e0d1b5d46914d14ef4602f2 and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is WILTROM CO., LTD..
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