Taiwan FDA registration 424b004c7b7617fb828a2f6e91c84dc8
"Maojing" blood collection needle (sterile)
TW: "茂晶" 採血針 (滅菌)
Registration details
- Analysis ID
- 424b004c7b7617fb828a2f6e91c84dc8
- Customs Code
- DHA09600263707
Company information
- Manufacturer Country
- China
- Authorized Representative
- Metalgen Biotechnology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Chinese goods;; Input;; QMS/QSD
Dates and status
- Registration Date
- Feb 16, 2016
- Expiry Date
- Feb 16, 2026
About this record
Access comprehensive regulatory information for "Maojing" blood collection needle (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 424b004c7b7617fb828a2f6e91c84dc8 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Metalgen Biotechnology 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