Taiwan FDA registration 722890d5c8b290c64f9a0e93724c5ef9
“joimax” Endovapor2 and accessories
TW: “脊美適”高頻電極及其附件
Taiwan·Risk Class 2·MD·JOIMAX GMBH·Registered Oct 16, 2017 – Oct 16, 2027ActiveRegistration details
- Analysis ID
- 722890d5c8b290c64f9a0e93724c5ef9
- License Form
- Ministry of Health Medical Device Import No. 030346
- Customs Code
- DHA05603034607
Company information
- Manufacturer
- JOIMAX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H4300 Electrocutors for endoscopes and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 16, 2017
- Expiry Date
- Oct 16, 2027
About this record
Access comprehensive regulatory information for “joimax” Endovapor2 and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 722890d5c8b290c64f9a0e93724c5ef9 and manufactured by JOIMAX GMBH. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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