Taiwan FDA registration bc5283c2691bf2a61cc18dd25e66775b

"Shujiang" Iron Reagent Set (Unsterilized)

TW: "朕江" 鐵試劑套組 (未滅菌)

Taiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered May 18, 2022 – May 18, 2027Active

Registration details

Analysis ID: bc5283c2691bf2a61cc18dd25e66775b

Company information

Manufacturer: LANNER BIOTECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: LANNER BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "Iron (Non-blood Matrix) Test System (A.1410)" 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.1410 Iron (non-blood matrix) testing system
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: May 18, 2022
Expiry Date: May 18, 2027

About this record

Access comprehensive regulatory information for "Shujiang" Iron Reagent Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bc5283c2691bf2a61cc18dd25e66775b and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..

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