Taiwan FDA registration 8a497949b364afa8f50cb7c31b05da89
“CMT” Vesica Kyphoplasty System
TW: “中央醫療”微賽克球囊椎體成形術套組
Taiwan·Risk Class 2·MD·CENTRAL MEDICAL TECHNOLOGIES INC.·Registered Jul 05, 2016 – Jul 05, 2026ExpiredRegistration details
- Analysis ID
- 8a497949b364afa8f50cb7c31b05da89
- License Form
- Ministry of Health Medical Device Manufacturing No. 005379
Company information
- Manufacturer
- CENTRAL MEDICAL TECHNOLOGIES INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- CENTRAL MEDICAL TECHNOLOGIES INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 05, 2016
- Expiry Date
- Jul 05, 2026
About this record
Access comprehensive regulatory information for “CMT” Vesica Kyphoplasty System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8a497949b364afa8f50cb7c31b05da89 and manufactured by CENTRAL MEDICAL TECHNOLOGIES INC.. The authorized representative in Taiwan is CENTRAL MEDICAL TECHNOLOGIES INC..
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