Taiwan FDA registration 1faf4fd69179d6f11de50243037a8c00

"Byo" platelet agglutination tester

TW: “拜歐”血小板凝集測定儀

Taiwan·Risk Class 2·BIO/DATA CORPORATION·Registered Sep 17, 2012 – Sep 17, 2027Active

Registration details

Analysis ID: 1faf4fd69179d6f11de50243037a8c00
Customs Code: DHA00602401505

Company information

Manufacturer: BIO/DATA CORPORATION
Manufacturer Country: United States
Authorized Representative: LORION ENTERPRISES INC.

Product details

Intended Use: It is used to determine the agglutination reaction of platelet-rich plasma (PRP) platelets after the addition of agglutination reaction agonists.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.6675 血小板凝集器
Import Information: import

Dates and status

Registration Date: Sep 17, 2012
Expiry Date: Sep 17, 2027

About this record

Access comprehensive regulatory information for "Byo" platelet agglutination tester in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1faf4fd69179d6f11de50243037a8c00 and manufactured by BIO/DATA CORPORATION. The authorized representative in Taiwan is LORION ENTERPRISES INC..

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