Taiwan FDA registration 3f7139830d01311db41c93b96d5cb140
Orien "Parory" urea/pylori reagent
TW: 歐銳恩"派羅瑞" 尿素/幽門桿菌試劑
Taiwan·Risk Class 1·ORION DIAGNOSTICA LTD·Registered Oct 26, 2005 – Oct 26, 2015CancelledRegistration details
- Analysis ID
- 3f7139830d01311db41c93b96d5cb140
- Customs Code
- DHA04400124900
Company information
- Manufacturer
- ORION DIAGNOSTICA LTD
- Manufacturer Country
- Finland
- Authorized Representative
- HOPE WANG ENTERPRISES CO., LTD.
Product details
- Intended Use
- Is it a rapid, eye-readable test for the detection of Helicobacter gastric urea in patient sections? activity.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0003 螺旋桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Oct 26, 2005
- Expiry Date
- Oct 26, 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 "Parory" urea/pylori reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f7139830d01311db41c93b96d5cb140 and manufactured by ORION DIAGNOSTICA LTD. The authorized representative in Taiwan is HOPE WANG ENTERPRISES CO., LTD..
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