Taiwan FDA registration 5964460c810f4e4207c3151bc976965f
"Vicks" Bone Filler Injection Tool Series (Sterilization)
TW: "維克疏" 骨填充物注入工具系列(滅菌)
Registration details
- Analysis ID
- 5964460c810f4e4207c3151bc976965f
- Customs Code
- DHY04300099000
Company information
- Manufacturer
- CENTRAL MEDICAL TECHNOLOGIES INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- CENTRAL MEDICAL TECHNOLOGIES INC.
Product details
- Intended Use
- Tools used when injecting bone cement into bone and vertebral spaces.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4200 Bone cement distributor
- Import Information
- import
Dates and status
- Registration Date
- Feb 24, 2006
- Expiry Date
- Feb 24, 2016
- Cancellation Date
- Apr 15, 2016
Cancellation information
- Status
- Logged out
- Reason
- 效能逾越等級範圍
About this record
Access comprehensive regulatory information for "Vicks" Bone Filler Injection Tool Series (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5964460c810f4e4207c3151bc976965f and manufactured by CENTRAL MEDICAL TECHNOLOGIES INC.. The authorized representative in Taiwan is CENTRAL MEDICAL TECHNOLOGIES INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices