Taiwan FDA registration 5089821154e14716cd60c8b776e2e406
“Alphatec” Helifix Interspinous Spacer System
TW: “阿伐泰克”海力菲斯椎間植入物
Taiwan·Risk Class 2·MD·ALPHATEC SPINE INC.·Registered Mar 26, 2014 – Mar 26, 2019CancelledRegistration details
- Analysis ID
- 5089821154e14716cd60c8b776e2e406
- License Form
- Ministry of Health Medical Device Import No. 025979
- Customs Code
- DHA05602597900
Company information
- Manufacturer
- ALPHATEC SPINE INC.
- Manufacturer Country
- United States
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3050 Spine correction fixation between the peduncle plates
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 26, 2014
- Expiry Date
- Mar 26, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Alphatec” Helifix Interspinous Spacer System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5089821154e14716cd60c8b776e2e406 and manufactured by ALPHATEC SPINE INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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