Taiwan FDA registration 19712893973c62ce93350644f1baa27c
"Meditech" Cast removal instrument (Non-Sterile)
TW: "愛塔克" 石膏拆除器械 (未滅菌)
Taiwan·Risk Class 1·MD·MEDITECH GROUP, LLC·Registered Aug 21, 2015 – Aug 21, 2020CancelledRegistration details
- Analysis ID
- 19712893973c62ce93350644f1baa27c
- License Form
- Ministry of Health Medical Device Import No. 015596
- Customs Code
- DHA09401559601
Company information
- Manufacturer
- MEDITECH GROUP, LLC
- Manufacturer Country
- United States
- Authorized Representative
- WELLONG INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N5960 Gypsum removal apparatus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 21, 2015
- Expiry Date
- Aug 21, 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 "Meditech" Cast removal 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 19712893973c62ce93350644f1baa27c and manufactured by MEDITECH GROUP, LLC. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..
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