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“Synthes” Arch Laminoplasty System - Taiwan Registration c05b40487480807eafaaac7c4957aef9

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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c05b40487480807eafaaac7c4957aef9
Registration Details
Taiwan FDA Registration: c05b40487480807eafaaac7c4957aef9
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Device Details

“Synthes” Arch Laminoplasty System
TW: “信迪思”亞克椎板成形術系統
Risk Class 2
MD

Registration Details

c05b40487480807eafaaac7c4957aef9

Ministry of Health Medical Device Import No. 029716

DHA05602971601

Company Information

Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3050 Spine correction fixation between the peduncle plates

Imported from abroad

Dates and Status

May 10, 2017

May 10, 2027