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"E-TAKE" EBV Test Kit (Non-Sterile) - Taiwan Registration 9005847b9df5bb70ca83c15956b997e4

Access comprehensive regulatory information for "E-TAKE" EBV Test Kit (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 9005847b9df5bb70ca83c15956b997e4 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is E-TAKE TECHNOLOGY CO., LTD..

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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9005847b9df5bb70ca83c15956b997e4
Registration Details
Taiwan FDA Registration: 9005847b9df5bb70ca83c15956b997e4
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Device Details

"E-TAKE" EBV Test Kit (Non-Sterile)
TW: "้†ซ้”" EB็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

9005847b9df5bb70ca83c15956b997e4

Ministry of Health Medical Device Import No. 013824

DHA09401382401

Company Information

United States

Product Details

C Immunology and microbiology devices

C3235 Epstein-Barr virus serum reagent

Imported from abroad

Dates and Status

Jan 29, 2014

Jan 29, 2019

Aug 02, 2019

Cancellation Information

Logged out

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