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"Centoxi" Heart Rhythm Regulator Repair Tool (Sterilization) - Taiwan Registration a7c156610fe664043a77b0152d2f9cb6

Access comprehensive regulatory information for "Centoxi" Heart Rhythm Regulator Repair Tool (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a7c156610fe664043a77b0152d2f9cb6 and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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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a7c156610fe664043a77b0152d2f9cb6
Registration Details
Taiwan FDA Registration: a7c156610fe664043a77b0152d2f9cb6
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Device Details

"Centoxi" Heart Rhythm Regulator Repair Tool (Sterilization)
TW: "็™พๅคšๅŠ›" ๅฟƒๅพ‹่ชฟ็ฏ€ๅ™จ็ถญไฟฎๅทฅๅ…ท (ๆป…่Œ)
Risk Class 1

Registration Details

a7c156610fe664043a77b0152d2f9cb6

DHA09401407606

Company Information

Germany

Product Details

It is limited to the first level of identification of cardiac rhythm regulator maintenance tools (E.3730) of the classification and grading management measures for medical equipment.

E Cardiovascular Medicine Science

E.3730 ๅฟƒๅพ‹่ชฟ็ฏ€ๅ™จ็ถญไฟฎๅทฅๅ…ท

Input;; QMS/QSD

Dates and Status

Apr 21, 2014

Apr 21, 2029