Taiwan FDA registration 24c91ca06ffc72e61d4865b52e0fefa7
Tenri needle moxibustion needle
TW: 天利針灸針
Taiwan·Risk Class 2·Jiangsu Tianxie Medical Instrument Co.,Ltd.·Registered Mar 06, 2019 – Mar 06, 2029ActiveRegistration details
- Analysis ID
- 24c91ca06ffc72e61d4865b52e0fefa7
- Customs Code
- DHA09200100103
Company information
- Manufacturer
- Jiangsu Tianxie Medical Instrument Co.,Ltd.
- Manufacturer Country
- China
- Authorized Representative
- GREEN HOPE CORPORATION
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
- Mar 06, 2019
- Expiry Date
- Mar 06, 2029
About this record
Access comprehensive regulatory information for Tenri needle moxibustion needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 24c91ca06ffc72e61d4865b52e0fefa7 and manufactured by Jiangsu Tianxie Medical Instrument Co.,Ltd.. The authorized representative in Taiwan is GREEN HOPE CORPORATION.
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