Taiwan FDA registration ea16c8a8f49ce04073c12df9d192d4e3

Vitronone body test piece (non-sterilized)

TW: 威創酮體試片 (未滅菌)

Taiwan·Risk Class 1·Taibo Technology Co., Ltd. five-stock factory·Registered Oct 15, 2024 – Oct 15, 2029Active

Registration details

Analysis ID: ea16c8a8f49ce04073c12df9d192d4e3

Company information

Manufacturer: Taibo Technology Co., Ltd. five-stock factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TAIDOC TECHNOLOGY CORPORATION

Product details

Intended Use: Limited to the scope of the first level of identification of the "Ketone (Non-quantitative) Test System (A.1435)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1435 Ketone (non-quantitative) testing system
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: Oct 15, 2024
Expiry Date: Oct 15, 2029

About this record

Access comprehensive regulatory information for Vitronone body test piece (non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ea16c8a8f49ce04073c12df9d192d4e3 and manufactured by Taibo Technology Co., Ltd. five-stock factory. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

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