Taiwan FDA registration 516107ea0c0019bdcc572e0c075e21fe
"Aikman" modular shoulder humeral system
TW: “艾克曼”模組化肩關節肱骨系統
Taiwan·Risk Class 2·ACUMED LLC.·Registered Apr 06, 2010 – Apr 06, 2015CancelledRegistration details
- Analysis ID
- 516107ea0c0019bdcc572e0c075e21fe
- Customs Code
- DHA00602088104
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.3690 Shoulder joint humerus (half shoulder) metal type cement-type supplement
- Import Information
- import
Dates and status
- Registration Date
- Apr 06, 2010
- Expiry Date
- Apr 06, 2015
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aikman" modular shoulder humeral system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 516107ea0c0019bdcc572e0c075e21fe 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