Taiwan FDA registration d7199d7e724636ff8f6dd55b673e25b7
"Ryder" Alomet artificial skeletal replacement
TW: “萊德”阿洛美特人工骨骼替代品
Registration details
- Analysis ID
- d7199d7e724636ff8f6dd55b673e25b7
- Customs Code
- DHA05603654201
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
- Jun 15, 2023
- Expiry Date
- Jun 15, 2028
About this record
Access comprehensive regulatory information for "Ryder" Alomet artificial skeletal replacement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d7199d7e724636ff8f6dd55b673e25b7 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.
Free DatabasePowered by Pure Global AI89,000+ Devices