Taiwan FDA registration bdb59dedb2e1cdece251a04d5d596c2b

Wuding urine tube fluid

TW: 五鼎尿液品管液

Taiwan·Risk Class 2·APEX BIOTECHNOLOGY CORPORATION·Registered Oct 24, 2023 – Oct 24, 2028Active

Registration details

Analysis ID: bdb59dedb2e1cdece251a04d5d596c2b

Company information

Manufacturer: APEX BIOTECHNOLOGY CORPORATION
Manufacturer Country: Taiwan, Province of China
Authorized Representative: APEX BIOTECHNOLOGY CORPORATION

Product details

Intended Use: This product is a quality control material substance with known concentration, which is used to monitor the quality control of the analysis of Wuding microalbumin reagent cassette, Wuding creatinine reagent cassette, and Wuding microalbumin/creatinine ratio reagent cassette, and needs to be used with Wuding four-in-one multi-function analyzer.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1660 Quality control materials (analytical and non-analytical)
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: Oct 24, 2023
Expiry Date: Oct 24, 2028

About this record

Access comprehensive regulatory information for Wuding urine tube fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bdb59dedb2e1cdece251a04d5d596c2b and manufactured by APEX BIOTECHNOLOGY CORPORATION. The authorized representative in Taiwan is APEX BIOTECHNOLOGY CORPORATION.

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