Taiwan FDA registration 2c74c7187ba5ae8cc9415d93ff128c9d
"AMFIT" Limb orthosis (Non-Sterile)
TW: "安適"肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·AMFIT INC.·Registered Oct 29, 2015 – Oct 29, 2020CancelledRegistration details
- Analysis ID
- 2c74c7187ba5ae8cc9415d93ff128c9d
- License Form
- Ministry of Health Medical Device Import No. 015798
- Customs Code
- DHA09401579800
Company information
- Manufacturer
- AMFIT INC.
- Manufacturer Country
- United States
- Authorized Representative
- INNOVATIVE HEALTHCARE LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 29, 2015
- Expiry Date
- Oct 29, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "AMFIT" Limb orthosis (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 2c74c7187ba5ae8cc9415d93ff128c9d and manufactured by AMFIT INC.. The authorized representative in Taiwan is INNOVATIVE HEALTHCARE LTD..
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