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"Kenedict" Fixing Molds & Accessories (Indepleted) - Taiwan Registration 9c38bfabc57719755c549ca3aab09e7e

Access comprehensive regulatory information for "Kenedict" Fixing Molds & Accessories (Indepleted) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9c38bfabc57719755c549ca3aab09e7e and manufactured by KINETEC SAS. The authorized representative in Taiwan is BLESSING CATHAY CORPORATION.

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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9c38bfabc57719755c549ca3aab09e7e
Registration Details
Taiwan FDA Registration: 9c38bfabc57719755c549ca3aab09e7e
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Device Details

"Kenedict" Fixing Molds & Accessories (Indepleted)
TW: "่‚ฏๅฐผๅธๅ…‹" ๅ›บๅฎš็”จๆจกๆๅŠ้…ไปถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9c38bfabc57719755c549ca3aab09e7e

DHA084A0029809

Company Information

France

Product Details

It is limited to the first level of identification of the classification and grading management of medical devices "splints for non-inflatable limbs (I.3910)".

I General, Plastic Surgery and Dermatology

I.3910 Clip board for non-bulging limbs

import

Dates and Status

Aug 12, 2024

Oct 31, 2025