Taiwan FDA registration 1a153da5e1b2db924d2235e38bfc5c4f

"Shujiang" lactate dehydrogenase reagent (unsterilized)

TW: "朕江" 乳酸脫氫酶試劑 (未滅菌)

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

Registration details

Analysis ID: 1a153da5e1b2db924d2235e38bfc5c4f

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 classification and grading management method of medical equipment "lactate dehydrogenase test system (A.1440)" level first level identification range.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1440 Lactate Dehydrogenase Test 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" lactate dehydrogenase reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1a153da5e1b2db924d2235e38bfc5c4f and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..

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