Taiwan FDA registration ceb279fac84677a6fcaa096710354bdd
"Esrith" Pushrak suture anchors
TW: “艾思瑞斯”普仕拉克縫合錨釘
Taiwan·Risk Class 2·ARTHREX INC.·Registered Aug 28, 2009 – Aug 28, 2029ActiveRegistration details
- Analysis ID
- ceb279fac84677a6fcaa096710354bdd
- Customs Code
- DHA00602014906
Company information
- Manufacturer
- ARTHREX INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- import
Dates and status
- Registration Date
- Aug 28, 2009
- Expiry Date
- Aug 28, 2029
About this record
Access comprehensive regulatory information for "Esrith" Pushrak suture anchors in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ceb279fac84677a6fcaa096710354bdd and manufactured by ARTHREX INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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