Taiwan FDA registration 40856a5d717555f06006d0b1f530212a

Longyi blood glucose test system

TW: 龍易血糖測試系統
Taiwan flagTaiwan·Risk Class 2·Taibo Technology Co., Ltd. five-stock factory·Registered Jun 24, 2011 – Jun 24, 2016Cancelled
Registration details
Analysis ID
40856a5d717555f06006d0b1f530212a
Customs Code
DHY00500330200
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
DRAGON PHARMACEUTICAL CO., LTD.
Product details
Intended Use
This product provides a quantitative blood glucose test, which is suitable for diabetic patients to self-measure blood sugar or medical professionals to measure blood sugar. This system is suitable for fresh microvascular blood for blood glucose detection.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1345 Glucose Test System
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Jun 24, 2011
Expiry Date
Jun 24, 2016
Cancellation Date
Aug 17, 2016
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Longyi 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 40856a5d717555f06006d0b1f530212a and manufactured by Taibo Technology Co., Ltd. five-stock factory. The authorized representative in Taiwan is DRAGON PHARMACEUTICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Longsheng Pharmaceutical Co., Ltd.;; Taibo Technology Co., Ltd. five stock factory, Taibo Technology Co., Ltd. five-stock factory, and 2 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.

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