Taiwan FDA registration 88ba3a32bbb481c5fd7f931ec72d4eae
"Nipro" hole needle combination
TW: “尼普洛”洞眼針組合
Taiwan·Risk Class 2·NIPRO CORPORATION ODATE FACTORY·Registered Dec 11, 2012 – Dec 11, 2027ActiveRegistration details
- Analysis ID
- 88ba3a32bbb481c5fd7f931ec72d4eae
- Customs Code
- DHA00602422707
Company information
- Manufacturer
- NIPRO CORPORATION ODATE FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- HUA CHIANG MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5540 Blood Access Devices and Accessories
- Import Information
- import
Dates and status
- Registration Date
- Dec 11, 2012
- Expiry Date
- Dec 11, 2027
About this record
Access comprehensive regulatory information for "Nipro" hole needle combination in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 88ba3a32bbb481c5fd7f931ec72d4eae and manufactured by NIPRO CORPORATION ODATE FACTORY. The authorized representative in Taiwan is HUA CHIANG MEDICAL 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