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"Smith" Protex nasopharyngeal airway tube (sterilized) - Taiwan Registration 030da99a28d0f440f32a345b0691e262

Access comprehensive regulatory information for "Smith" Protex nasopharyngeal airway tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 030da99a28d0f440f32a345b0691e262 and manufactured by SMITHS HEALTHCARE MANUFACTURING SA DE CV. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SMITHS HEALTHCARE MANUFACTURING SA DE CV, and 1 recent registrations in the same category. 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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030da99a28d0f440f32a345b0691e262
Registration Details
Taiwan FDA Registration: 030da99a28d0f440f32a345b0691e262
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Device Details

"Smith" Protex nasopharyngeal airway tube (sterilized)
TW: "ๅฒๅฏ†ๆ–ฏ" ไฟๅพทๅฃซ้ผปๅ’ฝๆฐฃ้“็ฎก (ๆป…่Œ)
Risk Class 1

Registration Details

030da99a28d0f440f32a345b0691e262

DHA09401604008

Company Information

Product Details

Limited to the classification and grading management of medical equipment "nasopharyngeal airway tube (D.5100)" level identification range.

D Anesthesiology

D.5100 Nasopharyngeal airway tubes

Input;; QMS/QSD

Dates and Status

Dec 31, 2015

Dec 31, 2025

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