"Nipro" plastic injection needle
Taiwan·Risk Class 2·NIPRO (SHANGHAI) CO., LTD.;; NIPRO CORPORATION·Registered Jan 20, 2009 – Jan 20, 2029Active- Analysis ID
- 886202a13edbfc05a917aadcd7f16d21
- Customs Code
- DHA04200019202
- Manufacturer
- NIPRO (SHANGHAI) CO., LTD.;; NIPRO CORPORATION
- Manufacturer Country
- Japan;;China
- Authorized Representative
- HUA CHIANG MEDICAL CO., LTD.
- 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
- Input;; Chinese goods
- Registration Date
- Jan 20, 2009
- Expiry Date
- Jan 20, 2029
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Access comprehensive regulatory information for "Nipro" plastic injection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 886202a13edbfc05a917aadcd7f16d21 and manufactured by NIPRO (SHANGHAI) CO., LTD.;; NIPRO CORPORATION. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIPRO (THAILAND) CORPORATION LIMITED, and 1 recent registrations in the same category. 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.