"Essens" rapid blood glucose test unit II
Taiwan·Risk Class 2·i-SENS, Wonju Factory·Registered Nov 02, 2010 – Nov 02, 2020Cancelled- Analysis ID
- 1c7ad21df98e2b6a5280ddf8f7ca6ec0
- Customs Code
- DHA00602167404
- Manufacturer
- i-SENS, Wonju Factory
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- I CHIANG INSTRUMENT CO., LTD.
- Intended Use
- Measure the concentration of glucose in the blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1345 Glucose Test System
- Registration Date
- Nov 02, 2010
- Expiry Date
- Nov 02, 2020
- Cancellation Date
- Jun 17, 2023
- Status
- Logged out
- Reason
- 許可證已逾有效期;;自行鍵入
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Access comprehensive regulatory information for "Essens" rapid blood glucose test unit II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c7ad21df98e2b6a5280ddf8f7ca6ec0 and manufactured by i-SENS, Wonju Factory. The authorized representative in Taiwan is I CHIANG INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including I – SENS, INC., and 1 recent registrations in the same category. 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.