Taiwan FDA registration 4ba98d54ff67c6839764b0e0b3c57ad8
"THERAGUN" Manual cast application and removal instrument (non-sterile)
TW: "特拉鋼" 手動式打石膏及拆石膏器械 (未滅菌)
Taiwan·Risk Class 1·MD·THERAGUN LLC·Registered Oct 19, 2017 – Oct 19, 2022ExpiredRegistration details
- Analysis ID
- 4ba98d54ff67c6839764b0e0b3c57ad8
- License Form
- Ministry of Health Medical Device Import No. 018429
- Customs Code
- DHA09401842907
Company information
- Manufacturer
- THERAGUN LLC
- Manufacturer Country
- United States
- Authorized Representative
- MEDEPOT CO., LTD
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Equipment "Manual Casting and Removal of Gypsum Removal Equipment (N.5980)".
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N5980 Manual plaster casting and plaster removal equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 19, 2017
- Expiry Date
- Oct 19, 2022
About this record
Access comprehensive regulatory information for "THERAGUN" Manual cast application and 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 4ba98d54ff67c6839764b0e0b3c57ad8 and manufactured by THERAGUN LLC. The authorized representative in Taiwan is MEDEPOT CO., LTD.
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