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"Aeon"Blood Cell Separation Kit - Taiwan Registration a184cef6b32cc73cd3e65813f6bb3a94

Access comprehensive regulatory information for "Aeon"Blood Cell Separation Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a184cef6b32cc73cd3e65813f6bb3a94 and manufactured by AEON BIOTHERAPEUTICS CORP.. The authorized representative in Taiwan is AEON BIOTHERAPEUTICS CORP..

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.

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a184cef6b32cc73cd3e65813f6bb3a94
Registration Details
Taiwan FDA Registration: a184cef6b32cc73cd3e65813f6bb3a94
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Device Details

"Aeon"Blood Cell Separation Kit
TW: "ไบžๆฉ"่ก€็ƒ็ดฐ่ƒžๅˆ†้›ข็ต„
Risk Class 2
MD

Registration Details

a184cef6b32cc73cd3e65813f6bb3a94

Ministry of Health Medical Device Manufacturing No. 005816

Company Information

Taiwan, Province of China

Product Details

This product can be taken by the patient and separated into red blood cells, white blood cells, plasma and platelets, etc., retaining platelet-rich plasma (PRP).

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Produced in Taiwan, China

Dates and Status

Jan 30, 2018

Jan 30, 2023