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"Kellos Martin" mandible fixed mesh - Taiwan Registration 25c4d74e644061c8042ffab5b0bf42eb

Access comprehensive regulatory information for "Kellos Martin" mandible fixed mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25c4d74e644061c8042ffab5b0bf42eb and manufactured by GEBRรœDER MARTIN GMBH & CO. KG;; Karl Leibinger Medizintechnik GmbH & Co. KG. The authorized representative in Taiwan is KLS MARTIN TAIWAN 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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25c4d74e644061c8042ffab5b0bf42eb
Registration Details
Taiwan FDA Registration: 25c4d74e644061c8042ffab5b0bf42eb
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Device Details

"Kellos Martin" mandible fixed mesh
TW: โ€œๅ‡ฑๆจ‚ๆ€้ฆฌไธโ€ไธ‹้ ท้ชจๅ›บ็ถฒ
Risk Class 2

Registration Details

25c4d74e644061c8042ffab5b0bf42eb

DHA05603163901

Product Details

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

F Dentistry

F.4760 Bone plates

import

Dates and Status

Sep 21, 2018

Sep 21, 2023