Taiwan FDA registration a7c156610fe664043a77b0152d2f9cb6

"Centoxi" Heart Rhythm Regulator Repair Tool (Sterilization)

TW: "百多力" 心律調節器維修工具 (滅菌)

Taiwan·Risk Class 1·BIOTRONIC SE & CO. KG·Registered Apr 21, 2014 – Apr 21, 2029Active

Registration details

Analysis ID: a7c156610fe664043a77b0152d2f9cb6
Customs Code: DHA09401407606

Company information

Manufacturer: BIOTRONIC SE & CO. KG
Manufacturer Country: Germany
Authorized Representative: BIOTRONIK TAIWAN LIMITED

Product details

Intended Use: 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.
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.3730 心律調節器維修工具
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Apr 21, 2014
Expiry Date: Apr 21, 2029

About this record

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.