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Pentax rigid laryngoscope blades (sterilized) - Taiwan Registration 169849cd295368594f102db6c23ff013

Access comprehensive regulatory information for Pentax rigid laryngoscope blades (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 169849cd295368594f102db6c23ff013 and manufactured by GALEMED CORPORATION. The authorized representative in Taiwan is GALEMED CORPORATION.

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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169849cd295368594f102db6c23ff013
Registration Details
Taiwan FDA Registration: 169849cd295368594f102db6c23ff013
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Device Details

Pentax rigid laryngoscope blades (sterilized)
TW: ใ€ๅด‡ไปใ€ž่ณ“ๅพ—ๅฃซ็กฌๅผๅ–‰้ ญ้ก่‘‰็‰‡ (ๆป…่Œ)
Risk Class 1

Registration Details

169849cd295368594f102db6c23ff013

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "rigid laryngoscope (D.5540)" of the Measures for the Classification and Grading Management of Medical Devices.

D Anesthesiology

D.5540 Rigid laryngoscope

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jan 04, 2013

Jan 04, 2028