Taiwan FDA registration f7c65f382616000c384fc10ca7aeea28
“DAIWHA” Meditom Electrosurgical unit
TW: “大華”麥德塔電刀系統
Taiwan·Risk Class 2·MD·Daiwha Corp., Ltd.·Registered Feb 03, 2023 – Feb 03, 2028ActiveRegistration details
- Analysis ID
- f7c65f382616000c384fc10ca7aeea28
- License Form
- Ministry of Health Medical Device Import No. 036297
- Customs Code
- DHA05603629701
Company information
- Manufacturer
- Daiwha Corp., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SOAR INSTRUMENT-TECH. CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 03, 2023
- Expiry Date
- Feb 03, 2028
About this record
Access comprehensive regulatory information for “DAIWHA” Meditom Electrosurgical unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f7c65f382616000c384fc10ca7aeea28 and manufactured by Daiwha Corp., Ltd.. The authorized representative in Taiwan is SOAR INSTRUMENT-TECH. CO., LTD..
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