Taiwan FDA registration 7f4b4ca60e336c8d6884ae15fd66367f

Beckman Coulter Insulin Reagent Set (non-sterile)

TW: 貝克曼庫爾特胰島素試劑組(未滅菌)

Taiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered Nov 04, 2024 – Nov 04, 2029Active

Registration details

Analysis ID: 7f4b4ca60e336c8d6884ae15fd66367f
Customs Code: DHA09402365803

Company information

Manufacturer: BECKMAN COULTER, INC.
Manufacturer Country: United States
Authorized Representative: BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)

Product details

Intended Use: It is limited to the first level of identification of the immune response insulin test system (A.1405) of the classification and grading management measures for medical devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1405 Immune Response Insulin Test System
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Nov 04, 2024
Expiry Date: Nov 04, 2029

About this record

Access comprehensive regulatory information for Beckman Coulter Insulin Reagent Set (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7f4b4ca60e336c8d6884ae15fd66367f and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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