Taiwan FDA registration ace44b0cf504af23e63c5b711b03a693
"Medical bone tolerance" injectable human demineralized bone matrix
TW: “醫骨耐”可注射式人類脫礦骨基質
Taiwan·Risk Class 2·Wright Medical Technology, Inc.·Registered Aug 22, 2023 – Aug 22, 2028ActiveRegistration details
- Analysis ID
- ace44b0cf504af23e63c5b711b03a693
- Customs Code
- DHA05603670105
Company information
- Manufacturer
- Wright Medical Technology, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Stryker (Far East) Co., Ltd. Taiwan Branch
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3045 Absorbable Calcium Salt Bone Cavity Filling Device
- Import Information
- import
Dates and status
- Registration Date
- Aug 22, 2023
- Expiry Date
- Aug 22, 2028
About this record
Access comprehensive regulatory information for "Medical bone tolerance" injectable human demineralized bone matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ace44b0cf504af23e63c5b711b03a693 and manufactured by Wright Medical Technology, Inc.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
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