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"Smith" Protex percutaneous trachetomy sleeve set - Taiwan Registration d07c18c1f687e3d9aae1599d9aaec912

Access comprehensive regulatory information for "Smith" Protex percutaneous trachetomy sleeve set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d07c18c1f687e3d9aae1599d9aaec912 and manufactured by Smiths Medical Czech Republic a.s.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.

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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d07c18c1f687e3d9aae1599d9aaec912
Registration Details
Taiwan FDA Registration: d07c18c1f687e3d9aae1599d9aaec912
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Device Details

"Smith" Protex percutaneous trachetomy sleeve set
TW: โ€œๅฒๅฏ†ๆ–ฏโ€ไฟๅพทๅฃซ็ถ“็šฎๅผๆฐฃๅˆ‡ๅฅ—็ฎก็ต„
Risk Class 2

Registration Details

d07c18c1f687e3d9aae1599d9aaec912

DHA00601863102

Company Information

Product Details

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

D Anesthesiology

D.5800 ๆฐฃๅˆ‡็ฎกๅŠๅ…ถๆฐฃๅ›Š

import

Dates and Status

Mar 07, 2008

Mar 07, 2028