Taiwan FDA registration 030da99a28d0f440f32a345b0691e262

"Smith" Protex nasopharyngeal airway tube (sterilized)

TW: "史密斯" 保德士鼻咽氣道管 (滅菌)
Taiwan flagTaiwan·Risk Class 1·SMITHS HEALTHCARE MANUFACTURING SA DE CV·Registered Dec 31, 2015 – Dec 31, 2025Expired
Registration details
Analysis ID
030da99a28d0f440f32a345b0691e262
Customs Code
DHA09401604008
Company information
Manufacturer Country
Mexico
Authorized Representative
RADIANT MEDICAL COMPANY
Product details
Intended Use
Limited to the classification and grading management of medical equipment "nasopharyngeal airway tube (D.5100)" level identification range.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5100 Nasopharyngeal airway tubes
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Dec 31, 2015
Expiry Date
Dec 31, 2025
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About this record

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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