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"Snowden Pencer" Speculum and Accessories (Non-Sterile) - Taiwan Registration 268a3b5dfb6efcb6e6c013636be79b72

Access comprehensive regulatory information for "Snowden Pencer" Speculum 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 268a3b5dfb6efcb6e6c013636be79b72 and manufactured by CAREFUSION. The authorized representative in Taiwan is DOUBLE-SUCCESS 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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268a3b5dfb6efcb6e6c013636be79b72
Registration Details
Taiwan FDA Registration: 268a3b5dfb6efcb6e6c013636be79b72
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Device Details

"Snowden Pencer" Speculum and Accessories (Non-Sterile)
TW: "ๅฒ่ซพ้ “่ณ“ๅฃซ" ๆชขๆŸฅ้กๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

268a3b5dfb6efcb6e6c013636be79b72

Ministry of Health Medical Device Import No. 016963

DHA09401696304

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Examination Scopes and Their Accessories (I.1800)".

I General and plastic surgical devices

I1800 inspection mirror and accessories

Imported from abroad

Dates and Status

Sep 06, 2016

Sep 06, 2021