Bayer Bycon blood glucose monitoring system
Taiwan·Risk Class 2·MANUFACTURED BY HTL-STREFA S.A. FOR BAYER HEALTHCARE LLC DIABETES CARE;; Manufactured by Panasonic Healthcare Co., Ltd. In Vitro Diagnostics Business Unit, Wakimachi Plant for Bayer Healthcare LLC;; MANUFACTURED BY KIMBALL ELECTRONICS FOR BAYER HEALTH CARE LLC, DIABETES CARE·Registered Feb 10, 2009 – Feb 10, 2019Cancelled- Analysis ID
- 61acaf71f9f41fbbfb268add55833482
- Customs Code
- DHA00601994300
- Manufacturer Country
- Thailand;;Poland;;Japan
- Authorized Representative
- Taiwan Bayer Co., Ltd
- Intended Use
- For diabetic patients to self-monitor their blood sugar, or for a health care professional to test the glucose concentration in whole blood.
- Product Type (Level 1)
- A Clinical Chemistry and Clinical Toxicology;; I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Manual instruments for general surgery; A.1345 Glucose Test System
- Import Information
- import
- Registration Date
- Feb 10, 2009
- Expiry Date
- Feb 10, 2019
- Cancellation Date
- Dec 28, 2017
- Status
- Logged out
- Reason
- 自請註銷
Access comprehensive regulatory information for Bayer Bycon blood glucose monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61acaf71f9f41fbbfb268add55833482 and manufactured by MANUFACTURED BY HTL-STREFA S.A. FOR BAYER HEALTHCARE LLC DIABETES CARE;; Manufactured by Panasonic Healthcare Co., Ltd. In Vitro Diagnostics Business Unit, Wakimachi Plant for Bayer Healthcare LLC;; MANUFACTURED BY KIMBALL ELECTRONICS FOR BAYER HEALTH CARE LLC, DIABETES CARE. 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.