Taiwan FDA registration 21f4a082ced95bee5cfceb7032b99500
"Termao" Yagani needle
TW: “泰爾茂”亞加尼針頭
Taiwan·Risk Class 2·Zhejiang Kindly Medical Devices Co., Ltd.·Registered May 25, 2013 – May 25, 2028ActiveRegistration details
- Analysis ID
- 21f4a082ced95bee5cfceb7032b99500
- Customs Code
- DHA04200053503
Company information
- Manufacturer
- Zhejiang Kindly Medical Devices Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- TERUMO TAIWAN MEDICAL 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.5570 Subcutaneous single-chamber needle
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- May 25, 2013
- Expiry Date
- May 25, 2028
About this record
Access comprehensive regulatory information for "Termao" Yagani needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21f4a082ced95bee5cfceb7032b99500 and manufactured by Zhejiang Kindly Medical Devices Co., Ltd.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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