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Syncope immunoglobulin fluorescent binder (unsterilized) - Taiwan Registration 88c5b73602684b220574c95a5301a87d

Access comprehensive regulatory information for Syncope immunoglobulin fluorescent binder (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88c5b73602684b220574c95a5301a87d and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..

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88c5b73602684b220574c95a5301a87d
Registration Details
Taiwan FDA Registration: 88c5b73602684b220574c95a5301a87d
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Device Details

Syncope immunoglobulin fluorescent binder (unsterilized)
TW: ๅ”ๅ…‹ๅ…็–ซ็ƒ่›‹็™ฝ่žขๅ…‰็ตๅˆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

88c5b73602684b220574c95a5301a87d

DHA04400884002

Company Information

Product Details

Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.

B Hematology, pathology, and genetics

B.4010 Reaction Reagents for General Purposes

import

Dates and Status

May 21, 2010

May 21, 2020

Aug 05, 2022

Cancellation Information

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