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"Dibo" Pixar plus casing - Taiwan Registration 6ec68f6da8eb12d899b9ee161170bda9

Access comprehensive regulatory information for "Dibo" Pixar plus casing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ec68f6da8eb12d899b9ee161170bda9 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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6ec68f6da8eb12d899b9ee161170bda9
Registration Details
Taiwan FDA Registration: 6ec68f6da8eb12d899b9ee161170bda9
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Device Details

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

Registration Details

6ec68f6da8eb12d899b9ee161170bda9

DHA00602294402

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 30, 2011

Nov 30, 2021

Oct 12, 2023

Cancellation Information

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