Taiwan FDA registration 374ef241e3c0623b5ddcd68636d74f4c
"Ryder" Osterti bone graft
TW: “萊德”奧斯特提骨移植物
Taiwan·Risk Class 3·Wright Medical Technology, Inc.·Registered Oct 13, 2023 – Oct 13, 2028ActiveRegistration details
- Analysis ID
- 374ef241e3c0623b5ddcd68636d74f4c
- Customs Code
- DHA05603680606
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
- Oct 13, 2023
- Expiry Date
- Oct 13, 2028
About this record
Access comprehensive regulatory information for "Ryder" Osterti bone graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 374ef241e3c0623b5ddcd68636d74f4c and manufactured by Wright Medical Technology, Inc.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
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.
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