Taiwan FDA registration c51edbbe8a60ac6855995d338547f2ee

"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 Jul 31, 2009 – Jul 31, 2014Cancelled
Registration details
Analysis ID
c51edbbe8a60ac6855995d338547f2ee
Customs Code
DHA04400795205
Company information
Manufacturer Country
Mexico
Authorized Representative
RADIANT MEDICAL COMPANY
Product details
Intended Use
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5100 Nasopharyngeal airway tubes
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jul 31, 2009
Expiry Date
Jul 31, 2014
Cancellation Date
Aug 15, 2014
Cancellation information
Status
Logged out
Reason
自請註銷
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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 c51edbbe8a60ac6855995d338547f2ee 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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