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"Dibo" casing - Taiwan Registration a131b7c27378bf972837028b0c549938

Access comprehensive regulatory information for "Dibo" casing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a131b7c27378bf972837028b0c549938 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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a131b7c27378bf972837028b0c549938
Registration Details
Taiwan FDA Registration: a131b7c27378bf972837028b0c549938
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Device Details

"Dibo" casing
TW: โ€œๅธๅฏถโ€ๅฅ—็ฎก
Risk Class 2
Cancelled

Registration Details

a131b7c27378bf972837028b0c549938

DHA00602281501

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

Sep 19, 2011

Sep 19, 2021

Oct 12, 2023

Cancellation Information

Logged out

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