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"Weida" temporary crown and bridge resin - Taiwan Registration 9ede22a2e3bc5e507b9deee4afe98b1a

Access comprehensive regulatory information for "Weida" temporary crown and bridge resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ede22a2e3bc5e507b9deee4afe98b1a 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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9ede22a2e3bc5e507b9deee4afe98b1a
Registration Details
Taiwan FDA Registration: 9ede22a2e3bc5e507b9deee4afe98b1a
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Device Details

"Weida" temporary crown and bridge resin
TW: โ€œๅ‰้”โ€ๆšซๆ™‚ๆ€ง็‰™ๅ† ๅŠ็‰™ๆฉ‹ๆจน่„‚
Risk Class 2

Registration Details

9ede22a2e3bc5e507b9deee4afe98b1a

DHA05602936906

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

Feb 15, 2017

Feb 15, 2027