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“CRANBERRY”Rubber Dam and Accessories(Non-Sterile) - Taiwan Registration 70c487b9d1299b85ea595a773f3b57d0

Access comprehensive regulatory information for “CRANBERRY”Rubber Dam and Accessories(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 70c487b9d1299b85ea595a773f3b57d0 and manufactured by CRANBERRY (M) SDN. BHD.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL 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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70c487b9d1299b85ea595a773f3b57d0
Registration Details
Taiwan FDA Registration: 70c487b9d1299b85ea595a773f3b57d0
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Device Details

“CRANBERRY”Rubber Dam and Accessories(Non-Sterile)
TW: “克朗貝里”橡皮障及其附件(未滅菌)
Risk Class 1
MD

Registration Details

70c487b9d1299b85ea595a773f3b57d0

Ministry of Health Medical Device Import Registration No. 009704

DHA08400970406

Company Information

Malaysia

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Rubber Dam and Its Accessories (F.6300)".

F Dental devices

F6300 rubber dam and its accessories

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026