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"Flexicare" Rigid Laryngoscope (Non-Sterile) - Taiwan Registration 064d29d3ed723adbfcaa3c0ca9336975

Access comprehensive regulatory information for "Flexicare" 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 064d29d3ed723adbfcaa3c0ca9336975 and manufactured by FLEXICARE MEDICAL LIMITED.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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064d29d3ed723adbfcaa3c0ca9336975
Registration Details
Taiwan FDA Registration: 064d29d3ed723adbfcaa3c0ca9336975
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Device Details

"Flexicare" Rigid Laryngoscope (Non-Sterile)
TW: "่ฒๅŠ›ๆ–ฏๅฏ" ็กฌๅผๅ–‰้ ญ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

064d29d3ed723adbfcaa3c0ca9336975

Ministry of Health Medical Device Import No. 017407

DHA09401740705

Company Information

United Kingdom

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

Jan 12, 2017

Jan 12, 2027