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"Dibo" Pixar casing - Taiwan Registration 05799698268092dfdb8da303f3efb778

Access comprehensive regulatory information for "Dibo" Pixar casing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 05799698268092dfdb8da303f3efb778 and manufactured by THIEBAUD S.A.S. The authorized representative in Taiwan is GALDERMA HONG KONG LIMITED, 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.

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05799698268092dfdb8da303f3efb778
Registration Details
Taiwan FDA Registration: 05799698268092dfdb8da303f3efb778
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Device Details

"Dibo" Pixar casing
TW: โ€œๅธๅฏถโ€็šฎๅ…‹ๆ–ฏๅฅ—็ฎก
Risk Class 2
Cancelled

Registration Details

05799698268092dfdb8da303f3efb778

DHA00602294208

Company Information

France

Product Details

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

J General hospital and personal use equipment

J.5570 Subcutaneous single-chamber needle

import

Dates and Status

Nov 29, 2011

Nov 29, 2021

Oct 12, 2023

Cancellation Information

Logged out

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