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"Kehao-style" Peritai Esp implant system - Taiwan Registration d7cb2d4bc7e7e3fb4c80b82eb6daccd5

Access comprehensive regulatory information for "Kehao-style" Peritai Esp implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d7cb2d4bc7e7e3fb4c80b82eb6daccd5 and manufactured by CLINICAL HOUSE EUROPE GMBH. The authorized representative in Taiwan is ARCHER MEDICAL TRADING CORP..

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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d7cb2d4bc7e7e3fb4c80b82eb6daccd5
Registration Details
Taiwan FDA Registration: d7cb2d4bc7e7e3fb4c80b82eb6daccd5
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Device Details

"Kehao-style" Peritai Esp implant system
TW: โ€œๅ…‹ๆตฉๅผโ€ๅŸน้‡Œๆณฐ่‰พๆ–ฏๆ™ฎๆค้ซ”็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

d7cb2d4bc7e7e3fb4c80b82eb6daccd5

DHA00602164905

Company Information

Switzerland

Product Details

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

F Dentistry

F.3640 Bone Implants

import

Dates and Status

May 05, 2011

Nov 09, 2015

Apr 25, 2018

Cancellation Information

Logged out

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