Taiwan FDA registration 035ae1ec6028953180541dc2be3cdb81
Vitex biochemical products glycohydrated hemoglobin reagents
TW: 維特司生化產品醣化血色素試劑
Registration details
- Analysis ID
- 035ae1ec6028953180541dc2be3cdb81
- Customs Code
- DHA00601529602
Company information
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS, INC
- Manufacturer Country
- United States
- Authorized Representative
- Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch
Product details
- Intended Use
- The concentration of heme and glycosylated hemoglobin in pretreated human blood was quantitatively determined to calculate the percentage of hemoglobin glycosylated.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7470 Analysis of glycosylated hemoglobin
- Import Information
- import
Dates and status
- Registration Date
- Dec 07, 2005
- Expiry Date
- Dec 07, 2010
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Vitex biochemical products glycohydrated hemoglobin reagents in Taiwan's medical device market through Pure Global AI's free database. is registered under number 035ae1ec6028953180541dc2be3cdb81 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
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