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“KaVo” Facebow (Non-Sterile) - Taiwan Registration 552994f7c662754bebdfaf8ecd4a1da2

Access comprehensive regulatory information for “KaVo” Facebow (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 552994f7c662754bebdfaf8ecd4a1da2 and manufactured by KAVO DENTAL GMBH. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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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552994f7c662754bebdfaf8ecd4a1da2
Registration Details
Taiwan FDA Registration: 552994f7c662754bebdfaf8ecd4a1da2
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Device Details

“KaVo” Facebow (Non-Sterile)
TW: “卡瓦” 頜與頜顳關節關係位置測量計(未滅菌)
Risk Class 1
MD

Registration Details

552994f7c662754bebdfaf8ecd4a1da2

Ministry of Health Medical Device Import No. 022306

DHA09402230606

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Jaw and Maxillotemporal Joint Relationship Position Meter (F.3220)".

F Dental devices

F3220 Jaw-temporal joint position gauge

Imported from abroad; GMP

Dates and Status

Feb 09, 2021

Feb 09, 2026