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"Weida" CapitaLand temporary resin restoration tooth - Taiwan Registration 1d5baa2b7a920d666a442e539088b9d4

Access comprehensive regulatory information for "Weida" CapitaLand temporary resin restoration tooth in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d5baa2b7a920d666a442e539088b9d4 and manufactured by VITA Zahnfabrik H. Rauter GmbH & CO. KG;; VITA Zahnfabrik H. Rauter GmbH & Co. KG. The authorized representative in Taiwan is TESCO DENTAL ASIA LIMITED TAIWAN BRANCH (H.K.).

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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1d5baa2b7a920d666a442e539088b9d4
Registration Details
Taiwan FDA Registration: 1d5baa2b7a920d666a442e539088b9d4
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Device Details

"Weida" CapitaLand temporary resin restoration tooth
TW: โ€œๅ‰้”โ€ๅ‡ฑๅพทๆšซๆ™‚ๆ€งๆจน่„‚ไฟฎๅพฉ็‰™ๆ
Risk Class 2

Registration Details

1d5baa2b7a920d666a442e539088b9d4

DHA00602367809

Product Details

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

F Dentistry

F.3770 ๆšซๆ™‚ๆ€ง็‰™ๅ† ๅŠ็‰™ๆฉ‹ๆจน่„‚

import

Dates and Status

Jun 20, 2012

Jun 20, 2027