Taiwan FDA registration 306014df894899ca707506480abd3142
“IDOMAN” Thermablate EAS
TW: “艾多門”子宮內膜消融系統
Taiwan·Risk Class 2·MD·Idoman Teoranta·Registered Sep 10, 2018 – Sep 10, 2023ExpiredRegistration details
- Analysis ID
- 306014df894899ca707506480abd3142
- License Form
- Ministry of Health Medical Device Import No. 031521
- Customs Code
- DHA05603152104
Company information
- Manufacturer
- Idoman Teoranta
- Manufacturer Country
- Ireland
- Authorized Representative
- ANDERSON MEDICAL SUPPLY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 10, 2018
- Expiry Date
- Sep 10, 2023
About this record
Access comprehensive regulatory information for “IDOMAN” Thermablate EAS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 306014df894899ca707506480abd3142 and manufactured by Idoman Teoranta. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY CO., LTD..
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