Taiwan FDA registration c032fff66dc8abf705b7f13f5b93d940
Uxiang needle
TW: 宇祥針灸針
Taiwan·Risk Class 2·SUZHOU MEDICAL APPLIANCE FACTORY·Registered Aug 15, 2011 – Aug 15, 2026ActiveRegistration details
- Analysis ID
- c032fff66dc8abf705b7f13f5b93d940
- Customs Code
- DHA04200038000
Company information
- Manufacturer
- SUZHOU MEDICAL APPLIANCE FACTORY
- Manufacturer Country
- China
- Authorized Representative
- COSMOS INTERNATIONAL SUPPLIES 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
- Contract manufacturing;; Chinese goods;; input
Dates and status
- Registration Date
- Aug 15, 2011
- Expiry Date
- Aug 15, 2026
About this record
Access comprehensive regulatory information for Uxiang needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c032fff66dc8abf705b7f13f5b93d940 and manufactured by SUZHOU MEDICAL APPLIANCE FACTORY. The authorized representative in Taiwan is COSMOS INTERNATIONAL SUPPLIES CO., LTD..
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