Taiwan FDA registration fd5ed5718bbf993de8ac3348d4f2e5c6
Orien "Rotales" rotavirus reagent
TW: 歐銳恩"羅塔列斯"輪狀病毒試劑
Taiwan·Risk Class 1·ORION DIAGNOSTICA LTD·Registered Oct 03, 2005 – Oct 03, 2015CancelledRegistration details
- Analysis ID
- fd5ed5718bbf993de8ac3348d4f2e5c6
- Customs Code
- DHA04400072103
Company information
- Manufacturer
- ORION DIAGNOSTICA LTD
- Manufacturer Country
- Finland
- Authorized Representative
- HOPE WANG ENTERPRISES CO., LTD.
Product details
- Intended Use
- Detection of rotavirus in the stool of patients with rotavirus gastroenteritis.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3405 Poliomyelitis virus serum reagent
- Import Information
- import
Dates and status
- Registration Date
- Oct 03, 2005
- Expiry Date
- Oct 03, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Orien "Rotales" rotavirus reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd5ed5718bbf993de8ac3348d4f2e5c6 and manufactured by ORION DIAGNOSTICA LTD. The authorized representative in Taiwan is HOPE WANG ENTERPRISES CO., LTD..
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