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"Smith" Bodez nasopharyngeal airway tube (sterilized) - Taiwan Registration 74458e005e715fdff595d7af6977511f

Access comprehensive regulatory information for "Smith" Bodez 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 74458e005e715fdff595d7af6977511f and manufactured by SMITHS MEDICAL INTERNATIONAL LTD.. 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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74458e005e715fdff595d7af6977511f
Registration Details
Taiwan FDA Registration: 74458e005e715fdff595d7af6977511f
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Device Details

"Smith" Bodez nasopharyngeal airway tube (sterilized)
TW: โ€œๅฒๅฏ†ๆ–ฏโ€ไฟๅพทๅฃซ้ผปๅ’ฝๆฐฃ้“็ฎก(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

74458e005e715fdff595d7af6977511f

DHA04400490000

Company Information

United Kingdom

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".

D Anesthesiology

D.5100 Nasopharyngeal airway tubes

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jul 11, 2006

Jul 11, 2011

Nov 16, 2012

Cancellation Information

Logged out

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