Taiwan FDA registration 0320d8148b64fc2b97eb25f3260ae2de
Blood Glucose Card X-Blood Glucose Test System
TW: 血糖卡 X-血糖測試系統
Registration details
- Analysis ID
- 0320d8148b64fc2b97eb25f3260ae2de
- Customs Code
- DHA00601870301
Company information
- Manufacturer
- ARKRAY FACTORY INC.
- Manufacturer Country
- Japan
- Authorized Representative
- MED PHAR ENTERPRISE CO., LTD.
Product details
- Intended Use
- Measure glucose motance in fingerstick whole blood (WB).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1345 Glucose Test System
- Import Information
- import
Dates and status
- Registration Date
- Dec 25, 2007
- Expiry Date
- Dec 25, 2012
- Cancellation Date
- Mar 31, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Blood Glucose Card X-Blood Glucose Test System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0320d8148b64fc2b97eb25f3260ae2de and manufactured by ARKRAY FACTORY INC.. The authorized representative in Taiwan is MED PHAR ENTERPRISE 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.
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