Taiwan FDA registration fdab3873c5a6c7fa9c2348042a6e3ae9
"IMEDICOM" Orthopedic manual surgical instrument (Non-Sterile)
TW: "艾美康" 手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·IMEDICOM CO., LTD.·Registered May 11, 2016 – May 11, 2021CancelledRegistration details
- Analysis ID
- fdab3873c5a6c7fa9c2348042a6e3ae9
- License Form
- Ministry of Health Medical Device Import No. 016519
- Customs Code
- DHA09401651901
Company information
- Manufacturer
- IMEDICOM CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MYWAY INTERNATIONAL CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N4540 Manual osteologic surgery instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 11, 2016
- Expiry Date
- May 11, 2021
- Cancellation Date
- Jun 18, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "IMEDICOM" Orthopedic manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fdab3873c5a6c7fa9c2348042a6e3ae9 and manufactured by IMEDICOM CO., LTD.. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..
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