Taiwan FDA registration 1fb52da363b743ca7b647f07cc59f21d
Fore quality control fluid
TW: 福爾品管液
Taiwan·Risk Class 1·BIONOSTICS, INC·Registered Jul 01, 2009 – Jul 01, 2014CancelledRegistration details
- Analysis ID
- 1fb52da363b743ca7b647f07cc59f21d
- Customs Code
- DHA04400786803
Company information
- Manufacturer
- BIONOSTICS, INC
- Manufacturer Country
- United States
- Authorized Representative
- TAIDOC TECHNOLOGY CORPORATION
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)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Jul 01, 2009
- Expiry Date
- Jul 01, 2014
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Fore quality control fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1fb52da363b743ca7b647f07cc59f21d and manufactured by BIONOSTICS, INC. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.
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