Taiwan FDA registration c05b40487480807eafaaac7c4957aef9
“Synthes” Arch Laminoplasty System
TW: “信迪思”亞克椎板成形術系統
Taiwan·Risk Class 2·MD·SYNTHES GMBH·Registered May 10, 2017 – May 10, 2027ActiveRegistration details
- Analysis ID
- c05b40487480807eafaaac7c4957aef9
- License Form
- Ministry of Health Medical Device Import No. 029716
- Customs Code
- DHA05602971601
Company information
- Manufacturer
- SYNTHES GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN 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)
- N3050 Spine correction fixation between the peduncle plates
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 10, 2017
- Expiry Date
- May 10, 2027
About this record
Access comprehensive regulatory information for “Synthes” Arch Laminoplasty System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c05b40487480807eafaaac7c4957aef9 and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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