Taiwan FDA registration cc71fcae8868476261cfb0aa9adf6fd8
“Terumo” Neolus Needle
TW: “泰爾茂” 尼歐拉斯注射針
Taiwan·Risk Class 2·MD·TERUMO EUROPE N.V.·Registered May 12, 2021 – May 12, 2026ExpiredRegistration details
- Analysis ID
- cc71fcae8868476261cfb0aa9adf6fd8
- License Form
- Ministry of Health Medical Device Import No. 034523
- Customs Code
- DHA05603452300
Company information
- Manufacturer
- TERUMO EUROPE N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5570 Subcutaneous single-lumen needle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 12, 2021
- Expiry Date
- May 12, 2026
About this record
Access comprehensive regulatory information for “Terumo” Neolus Needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc71fcae8868476261cfb0aa9adf6fd8 and manufactured by TERUMO EUROPE N.V.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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