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"Medtronic" Sherpa guide tube - Taiwan Registration 76e268fbb96f7555d3a4888f43c3aad4

Access comprehensive regulatory information for "Medtronic" Sherpa guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 76e268fbb96f7555d3a4888f43c3aad4 and manufactured by MEDTRONIC VASCULAR. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC VASCULAR, and 1 recent registrations in the same category. 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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76e268fbb96f7555d3a4888f43c3aad4
Registration Details
Taiwan FDA Registration: 76e268fbb96f7555d3a4888f43c3aad4
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Device Details

"Medtronic" Sherpa guide tube
TW: โ€œ็พŽๆ•ฆๅŠ›โ€้›ช็ˆพๅธ•ๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

76e268fbb96f7555d3a4888f43c3aad4

DHA00601873402

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order.

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Mar 18, 2008

Mar 18, 2023

Jan 02, 2020

Cancellation Information

Logged out

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