Taiwan FDA registration f5c18d4d5e9cbf1e861599955eeb01b2

Lekang blood glucose testing system

TW: 樂康血糖測試系統

Taiwan·Risk Class 2·ACON LABORATORIES, INC.·Registered Nov 19, 2013 – Nov 19, 2023Expired

Registration details

Analysis ID: f5c18d4d5e9cbf1e861599955eeb01b2
Customs Code: DHA05602554802

Company information

Manufacturer: ACON LABORATORIES, INC.
Manufacturer Country: United States
Authorized Representative: FOCUS MEDICAL SYSTEM CORP.

Product details

Intended Use: Quantitatively detect the blood glucose value of fingertips, palms and forearm microvascular whole blood, and professional medical personnel can detect the blood glucose value of neonatal microvascular whole blood.
Product Type (Level 1): I General, Plastic Surgery & Dermatology;; A Clinical Chemistry and Clinical Toxicology
Product Type (Level 2): I.4800 Manual instruments for general surgery; A.1345 Glucose Test System
Import Information: import

Dates and status

Registration Date: Nov 19, 2013
Expiry Date: Nov 19, 2023

About this record

Access comprehensive regulatory information for Lekang blood glucose testing system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5c18d4d5e9cbf1e861599955eeb01b2 and manufactured by ACON LABORATORIES, INC.. The authorized representative in Taiwan is FOCUS MEDICAL SYSTEM CORP..

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