"貝克曼庫爾特" C-胜肽檢驗試劑(未滅菌) - Taiwan Registration 2968600f87b4f80acb1f9c94aeb9e235
Access comprehensive regulatory information for "貝克曼庫爾特" C-胜肽檢驗試劑(未滅菌) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2968600f87b4f80acb1f9c94aeb9e235 and manufactured by BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD.;; BECKMAN COULTER INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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Device Details
Registration Details
2968600f87b4f80acb1f9c94aeb9e235
DHA09600496001
Product Details
It is limited to the first level of identification of the insulin preplasm C-peptide test system (A.1135) of the classification and grading management measures for medical devices.
A Clinical chemistry and clinical toxicology
A.1135 胰島素前質C-肽類試驗系統
QMS/QSD;; Input;; Chinese goods
Dates and Status
Jul 08, 2024
Jul 08, 2029