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“Rusch” PercuQuick One-Step Dilator Set - Taiwan Registration 11277a78e77748a1df2a6df2d5438ea0

Access comprehensive regulatory information for “Rusch” PercuQuick One-Step Dilator Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 11277a78e77748a1df2a6df2d5438ea0 and manufactured by Teleflex Medical Sdn.Bhd. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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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11277a78e77748a1df2a6df2d5438ea0
Registration Details
Taiwan FDA Registration: 11277a78e77748a1df2a6df2d5438ea0
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Device Details

“Rusch” PercuQuick One-Step Dilator Set
TW: “路希”快速經皮氣切組
Risk Class 2
MD
Cancelled

Registration Details

11277a78e77748a1df2a6df2d5438ea0

Ministry of Health Medical Device Import No. 027841

DHA05602784107

Company Information

Malaysia

Product Details

D Devices for anesthesiology

D5800 Trachetomy tube and its balloon

Imported from abroad

Dates and Status

Nov 05, 2015

Nov 05, 2020

Jun 07, 2022

Cancellation Information

Logged out

許可證已逾有效期