Taiwan FDA registration 181ee5e1d2ed37aa9af8735fd3e91de3
Uko needle moxibustion needle
TW: 宇光針灸針
Taiwan·Risk Class 2·SHANGHAI YANGLONG MEDICAL ARTICLES CO., LTD.·Registered Mar 03, 2009 – Mar 03, 2014CancelledRegistration details
- Analysis ID
- 181ee5e1d2ed37aa9af8735fd3e91de3
- Customs Code
- DHA04200019301
Company information
- Manufacturer
- SHANGHAI YANGLONG MEDICAL ARTICLES CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- YU Kuang Industrial 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
- Mar 03, 2009
- Expiry Date
- Mar 03, 2014
- Cancellation Date
- Dec 14, 2016
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延
About this record
Access comprehensive regulatory information for Uko 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 181ee5e1d2ed37aa9af8735fd3e91de3 and manufactured by SHANGHAI YANGLONG MEDICAL ARTICLES CO., LTD.. The authorized representative in Taiwan is YU Kuang Industrial CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices