Taiwan FDA registration 91e8a147cb4be9a198a1b6347fea789a
"Bayer" STA buffer
TW: "拜耳"STA緩衝液
Registration details
- Analysis ID
- 91e8a147cb4be9a198a1b6347fea789a
- Customs Code
- DHA04400316300
Company information
- Manufacturer
- STAGO DIAGNOSTICS
- Manufacturer Country
- France
- Authorized Representative
- Taiwan Bayer Co., Ltd
Product details
- Intended Use
- In coagulation tests, dilution reagents or blood samples from patients.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4010 Reaction Reagents for General Purposes
- Import Information
- import
Dates and status
- Registration Date
- Mar 24, 2006
- Expiry Date
- Mar 24, 2011
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bayer" STA buffer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91e8a147cb4be9a198a1b6347fea789a and manufactured by STAGO DIAGNOSTICS. The authorized representative in Taiwan is Taiwan Bayer 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