Taiwan FDA registration faa1bbd7cbc046471fddcfce8da4f19e
Iveomec single-use sterile acupuncture needles
TW: 唯得美一次性使用無菌針灸針
Taiwan·Risk Class 2·WUXI ZHUSHI ACUPUNCTURE AND MOXIBUSTION SUPPLIES FACTORY·Registered Apr 02, 2010 – Apr 02, 2025ExpiredRegistration details
- Analysis ID
- faa1bbd7cbc046471fddcfce8da4f19e
- Customs Code
- DHA04200025408
Company information
- Manufacturer Country
- China
- Authorized Representative
- ARTURO INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5580 Needle moxibustion needle
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 02, 2010
- Expiry Date
- Apr 02, 2025
About this record
Access comprehensive regulatory information for Iveomec single-use sterile acupuncture needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number faa1bbd7cbc046471fddcfce8da4f19e and manufactured by WUXI ZHUSHI ACUPUNCTURE AND MOXIBUSTION SUPPLIES FACTORY. The authorized representative in Taiwan is ARTURO INSTRUMENTS CO., LTD..
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