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“Kerr” OptiBond eXTRa Universal - Taiwan Registration 0d7cff5795a1c0b0f1d4528e873f9092

Access comprehensive regulatory information for “Kerr” OptiBond eXTRa Universal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d7cff5795a1c0b0f1d4528e873f9092 and manufactured by KERR CORPORATION. The authorized representative in Taiwan is NOBEL BIOCARE TAIWAN 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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0d7cff5795a1c0b0f1d4528e873f9092
Registration Details
Taiwan FDA Registration: 0d7cff5795a1c0b0f1d4528e873f9092
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Device Details

“Kerr” OptiBond eXTRa Universal
TW: “科爾”歐邦艾拉自蝕黏著劑
Risk Class 2
MD

Registration Details

0d7cff5795a1c0b0f1d4528e873f9092

Ministry of Health Medical Device Import No. 033858

DHA05603385800

Company Information

United States

Product Details

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

F Dental devices

F3200 resin dental adhesive

Imported from abroad

Dates and Status

Sep 17, 2020

Sep 17, 2025