Taiwan FDA registration c191c708bf1c3e507d91782c02caa514
"Baiyiji" disposable anti-puncture venous lancet
TW: “百易吉” 一次性使用防針刺靜脈採血針
Taiwan·Risk Class 2·Yangzhou Medline Industry Co., Ltd.·Registered Sep 21, 2023 – Sep 21, 2028ActiveRegistration details
- Analysis ID
- c191c708bf1c3e507d91782c02caa514
- Customs Code
- DHA09200145707
Company information
- Manufacturer
- Yangzhou Medline Industry Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- Taiwan Buy1z Technology 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)
- J.5570 Subcutaneous single-chamber needle
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Sep 21, 2023
- Expiry Date
- Sep 21, 2028
About this record
Access comprehensive regulatory information for "Baiyiji" disposable anti-puncture venous lancet in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c191c708bf1c3e507d91782c02caa514 and manufactured by Yangzhou Medline Industry Co., Ltd.. The authorized representative in Taiwan is Taiwan Buy1z Technology Co., Ltd..
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