Taiwan FDA registration 358098930face3e02815e6f1cd5bb9a6

"SunMed" Rigid Laryngoscope (Non-Sterile)

TW: "三美德" 硬式喉頭鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SUNMED LLC·Registered Dec 11, 2015 – Dec 11, 2025Expired
Registration details
Analysis ID
358098930face3e02815e6f1cd5bb9a6
License Form
Ministry of Health Medical Device Import No. 015957
Customs Code
DHA09401595704
Company information
Manufacturer
SUNMED LLC
Manufacturer Country
United States
Authorized Representative
XIN BO ENTERPRISE CO., LTD.
Product details
Intended Use
Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5540 Rigid laryngoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 11, 2015
Expiry Date
Dec 11, 2025
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About this record

Access comprehensive regulatory information for "SunMed" Rigid Laryngoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 358098930face3e02815e6f1cd5bb9a6 and manufactured by SUNMED LLC. The authorized representative in Taiwan is XIN BO ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SUNMED LLC, 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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