Taiwan FDA registration a964d51d950e12dbc6d8c0f43d401ce5

"Shujiang" Microalbumin Reagent Set (Unsterilized)

TW: "朕江" 微量白蛋白試劑套組 (未滅菌)

Taiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered Jul 21, 2022 – Jul 21, 2027Active

Registration details

Analysis ID: a964d51d950e12dbc6d8c0f43d401ce5

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 of medical equipment "albumin immunoassay system (C.5040)" first level recognition range.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.5040 白蛋白免疫試驗系統
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: Jul 21, 2022
Expiry Date: Jul 21, 2027

About this record

Access comprehensive regulatory information for "Shujiang" Microalbumin 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 a964d51d950e12dbc6d8c0f43d401ce5 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.