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"SunMed" Rigid Laryngoscope (Non-Sterile) - Taiwan Registration 358098930face3e02815e6f1cd5bb9a6

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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358098930face3e02815e6f1cd5bb9a6
Registration Details
Taiwan FDA Registration: 358098930face3e02815e6f1cd5bb9a6
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Device Details

"SunMed" Rigid Laryngoscope (Non-Sterile)
TW: "ไธ‰็พŽๅพท" ็กฌๅผๅ–‰้ ญ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

358098930face3e02815e6f1cd5bb9a6

Ministry of Health Medical Device Import No. 015957

DHA09401595704

Company Information

United States

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".

D Devices for anesthesiology

D5540 Rigid laryngoscope

Imported from abroad

Dates and Status

Dec 11, 2015

Dec 11, 2025

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