Taiwan FDA registration 3956c1efb13757ab52ddf210356b19ba
Orien "Peroria" dry pylori reagent
TW: 歐銳恩〝派羅瑞〞乾式幽門桿菌試劑
Taiwan·Risk Class 1·ORION DIAGNOSTICA LTD·Registered Oct 26, 2005 – Oct 26, 2015CancelledRegistration details
- Analysis ID
- 3956c1efb13757ab52ddf210356b19ba
- Customs Code
- DHA04400124808
Company information
- Manufacturer
- ORION DIAGNOSTICA LTD
- Manufacturer Country
- Finland
- Authorized Representative
- HOPE WANG ENTERPRISES CO., LTD.
Product details
- Intended Use
- Latex rapid agglutination was used to qualitatively detect Helicobacter pylobacter antibodies in human serum.
- 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 "Peroria" dry 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 3956c1efb13757ab52ddf210356b19ba and manufactured by ORION DIAGNOSTICA LTD. The authorized representative in Taiwan is HOPE WANG ENTERPRISES 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