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"Kentley" pulp rinse syringe - Taiwan Registration bb9cc4db9617663ee9e49e2edbdf955e

Access comprehensive regulatory information for "Kentley" pulp rinse syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bb9cc4db9617663ee9e49e2edbdf955e and manufactured by KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP. The authorized representative in Taiwan is Taiwan Tyco Pharmaceutical Co., 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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bb9cc4db9617663ee9e49e2edbdf955e
Registration Details
Taiwan FDA Registration: bb9cc4db9617663ee9e49e2edbdf955e
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Device Details

"Kentley" pulp rinse syringe
TW: "่‚ฏ็‰นๅˆฉ"็‰™้ซ“ๆฒ–ๆด—ๆณจๅฐ„ๅ™จ
Risk Class 1
Cancelled

Registration Details

bb9cc4db9617663ee9e49e2edbdf955e

DHA04400296502

Company Information

Product Details

Hand dental instruments are hand-held instruments used to perform various procedures in general dentistry and oral surgery.

F Dentistry

F.4565 ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ

import

Dates and Status

Mar 15, 2006

Mar 15, 2011

Jan 18, 2013

Cancellation Information

Logged out

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