Taiwan FDA registration 24fd94fdbcfc64f934af6de7b22698bf
"Nipro" Nipro blood passer
TW: "尼普洛"尼普洛血液過瀘器
Registration details
- Analysis ID
- 24fd94fdbcfc64f934af6de7b22698bf
- Customs Code
- DHA00600798704
Company information
- Manufacturer
- Nipro Corporation Odate Factory
- Manufacturer Country
- Japan
- Authorized Representative
- HUA CHIANG MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- 0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Sep 06, 1996
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for "Nipro" Nipro blood passer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 24fd94fdbcfc64f934af6de7b22698bf 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