Taiwan FDA registration 2d57413e0bbace8d9d8b3d5fb94af8f0
CHRONO-LOG Chrono-PAR #384 ADP Reagent
TW: 克羅隆格腺核苷二磷酸
Registration details
- Analysis ID
- 2d57413e0bbace8d9d8b3d5fb94af8f0
- License Form
- Department of Health Medical Device Import No. 014917
- Customs Code
- DHA00601491700
Company information
- Manufacturer
- CHRONO-LOG CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GRANT TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Determination of platelet function and secretory function in whole blood and platelet thick plasma.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B7040 Discharge analysis of glands triphosphate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 22, 2005
- Expiry Date
- Nov 22, 2025
About this record
Access comprehensive regulatory information for CHRONO-LOG Chrono-PAR #384 ADP Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2d57413e0bbace8d9d8b3d5fb94af8f0 and manufactured by CHRONO-LOG CORPORATION. The authorized representative in Taiwan is GRANT TECHNOLOGY 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