Taiwan FDA registration f750f9b951db0aa8837942e222e33ac8

"Daji" throat mask (sterilized)

TW: "達吉" 喉頭面罩 (滅菌)
Taiwan flagTaiwan·Risk Class 1·THE LARYNGEAL MASK COMPANY (SINGAPORE) PTE. LTD.·Registered Apr 13, 2012 – Apr 13, 2017Cancelled
Registration details
Analysis ID
f750f9b951db0aa8837942e222e33ac8
Customs Code
DHA04401159509
Company information
Manufacturer Country
Singapore
Authorized Representative
Hehua Co., Ltd
Product details
Intended Use
Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
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
Apr 13, 2012
Expiry Date
Apr 13, 2017
Cancellation Date
Sep 10, 2018
Cancellation information
Status
Logged out
Reason
公司歇業
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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 f750f9b951db0aa8837942e222e33ac8 and manufactured by THE LARYNGEAL MASK COMPANY (SINGAPORE) PTE. LTD.. The authorized representative in Taiwan is Hehua Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including THE LARYNGEAL MASK COMPANY (M) SDN. BHD., 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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