Taiwan FDA registration e8835c8e779402059514789deb966ba2

Boston Tech Seeker Suite

TW: “波士頓科技”導引器套組

Taiwan·Risk Class 2·GREATBATCH MEDICAL, S. DE R.L. DE C.V.; GREATBATCH MEDICAL INC·Registered Aug 10, 2020 – Aug 10, 2025Expired

Registration details

Analysis ID: e8835c8e779402059514789deb966ba2
Customs Code: DHA05603388207

Company information

Manufacturer: GREATBATCH MEDICAL, S. DE R.L. DE C.V.; GREATBATCH MEDICAL INC
Manufacturer Country: Mexico;;United States
Authorized Representative: Dutch Boston Technology Co., Ltd. Taiwan Branch

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.1340 Catheter Introducers
Import Information: import

Dates and status

Registration Date: Aug 10, 2020
Expiry Date: Aug 10, 2025

About this record

Access comprehensive regulatory information for Boston Tech Seeker Suite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e8835c8e779402059514789deb966ba2 and manufactured by GREATBATCH MEDICAL, S. DE R.L. DE C.V.; GREATBATCH MEDICAL INC. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.

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.