Taiwan FDA registration b413c61b121a5233e3e0b16d107776b8
"Aimi Fue Yasu" Manual osteologic surgical instrument (sterilization)
TW: "愛美笛康" 手動式骨科手術器械 (滅菌)
Registration details
- Analysis ID
- b413c61b121a5233e3e0b16d107776b8
- Customs Code
- DHA09401692203
Company information
- Manufacturer
- IMEDICOM CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EULOGIUMS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Aug 24, 2016
- Expiry Date
- Aug 24, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Aimi Fue Yasu" Manual osteologic surgical instrument (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b413c61b121a5233e3e0b16d107776b8 and manufactured by IMEDICOM CO., LTD.. The authorized representative in Taiwan is EULOGIUMS 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