Taiwan FDA registration 5d8303bc5cd8a04f2a4e1fb8ec2b14e4
"Nova" Hemoglobin control solution (Non-Sterile)
TW: "露華" 血紅素品管液 (未滅菌)
Registration details
- Analysis ID
- 5d8303bc5cd8a04f2a4e1fb8ec2b14e4
- License Form
- Ministry of Health Medical Device Import No. 018852
- Customs Code
- DHA09401885205
Company information
- Manufacturer
- NOVA BIOMEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- NOVA BIOMEDICAL TAIWAN CORP.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 02, 2018
- Expiry Date
- Mar 02, 2023
About this record
Access comprehensive regulatory information for "Nova" Hemoglobin control solution (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5d8303bc5cd8a04f2a4e1fb8ec2b14e4 and manufactured by NOVA BIOMEDICAL CORPORATION. The authorized representative in Taiwan is NOVA BIOMEDICAL TAIWAN CORP..
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