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"Mireil" Plano titanium alloy non-absorbable fixtures - Taiwan Registration a936f5161f1564551854135a9dfe6dd0

Access comprehensive regulatory information for "Mireil" Plano titanium alloy non-absorbable fixtures in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a936f5161f1564551854135a9dfe6dd0 and manufactured by Meril Endo Surgery Pvt. Ltd. The authorized representative in Taiwan is K&C MEDICAL 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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a936f5161f1564551854135a9dfe6dd0
Registration Details
Taiwan FDA Registration: a936f5161f1564551854135a9dfe6dd0
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Device Details

"Mireil" Plano titanium alloy non-absorbable fixtures
TW: โ€œๆธผ็‘ž็ˆพโ€ๆ™ฎๆœ—้ˆฆๅˆ้‡‘ไธๅฏๅธๆ”ถๅ›บๅฎš่ฃ็ฝฎ
Risk Class 2

Registration Details

a936f5161f1564551854135a9dfe6dd0

DHA05603761201

Company Information

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4750 Implantable Joints

import

Dates and Status

Oct 01, 2024

Oct 01, 2029