Taiwan FDA registration 6e36dfb6784f7439578b160b572b2488
Respiratory Viral Culture Cells (Unsterilized)
TW: 〝海柏〞呼吸道病毒培養細胞 (未滅菌)
Taiwan·Risk Class 1·DIAGNOSTIC HYBRIDS INCORPORATION·Registered May 23, 2012 – May 23, 2022CancelledRegistration details
- Analysis ID
- 6e36dfb6784f7439578b160b572b2488
- Customs Code
- DHA04401173601
Company information
- Manufacturer
- DIAGNOSTIC HYBRIDS INCORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GLOWAY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures "Cultured animals and human cells (B.2280)".
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.2280 Cultured animal and human cells
- Import Information
- import
Dates and status
- Registration Date
- May 23, 2012
- Expiry Date
- May 23, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Respiratory Viral Culture Cells (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6e36dfb6784f7439578b160b572b2488 and manufactured by DIAGNOSTIC HYBRIDS INCORPORATION. The authorized representative in Taiwan is GLOWAY 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