Taiwan FDA registration f8c9c568df9885a243efff5f01f7b639
"Aikman" acromion collarbone suspension repair system
TW: “艾克曼”肩峰鎖骨懸吊修補系統
Taiwan·Risk Class 2·ACUMED LLC.·Registered Sep 23, 2013 – Sep 23, 2028ActiveRegistration details
- Analysis ID
- f8c9c568df9885a243efff5f01f7b639
- Customs Code
- DHA05602547409
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
- Sep 23, 2013
- Expiry Date
- Sep 23, 2028
About this record
Access comprehensive regulatory information for "Aikman" acromion collarbone suspension repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f8c9c568df9885a243efff5f01f7b639 and manufactured by ACUMED LLC.. The authorized representative in Taiwan is WONDERLAND CORPORATION.
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