Taiwan FDA registration 16085b2403c1387dc4955084ab4f5435
"Aikman" modular hand bone fusion system
TW: “艾克曼”模組化手骨融合系統
Taiwan·Risk Class 2·ACUMED LLC.·Registered Nov 24, 2009 – Nov 24, 2029ActiveRegistration details
- Analysis ID
- 16085b2403c1387dc4955084ab4f5435
- Customs Code
- DHA00602043000
Company information
- Manufacturer
- ACUMED LLC.
- Manufacturer Country
- United States
- Authorized Representative
- WONDERLAND CORPORATION
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
- Nov 24, 2009
- Expiry Date
- Nov 24, 2029
About this record
Access comprehensive regulatory information for "Aikman" modular hand bone fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16085b2403c1387dc4955084ab4f5435 and manufactured by ACUMED LLC.. The authorized representative in Taiwan is WONDERLAND CORPORATION.
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