Taiwan FDA registration a17927a097a035c8136b2f51cfe4ad90

"Daji" throat mask (sterilized)

TW: "達吉" 喉頭面罩 (滅菌)
Taiwan flagTaiwan·Risk Class 1·THE LARYNGEAL MASK COMPANY (M) SDN. BHD.·Registered Sep 28, 2012 – Sep 28, 2027Active
Registration details
Analysis ID
a17927a097a035c8136b2f51cfe4ad90
Customs Code
DHA04401221300
Company information
Manufacturer Country
Malaysia
Authorized Representative
TELEFLEX MEDICAL TAIWAN LTD.
Product details
Intended Use
Limited to the classification and grading management method of medical equipment, oropharyngeal airway canal (D.5110) first grade identification range.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5110 Oropharyngeal airway tubes
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Sep 28, 2012
Expiry Date
Sep 28, 2027
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About this record

Access comprehensive regulatory information for "Daji" throat mask (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a17927a097a035c8136b2f51cfe4ad90 and manufactured by THE LARYNGEAL MASK COMPANY (M) SDN. BHD.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including THE LARYNGEAL MASK COMPANY (SINGAPORE) PTE. LTD., 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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