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"NIHON KOHDEN" Video Intubation Flexible Laryngoscope (Non-sterile) - Taiwan Registration 2eaea80a99fbdaa9a174c3097c583102

Access comprehensive regulatory information for "NIHON KOHDEN" Video Intubation Flexible 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 2eaea80a99fbdaa9a174c3097c583102 and manufactured by NIHON KOHDEN CORPORATION. The authorized representative in Taiwan is PARAMOUNT LAND COMPANY LTD..

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2eaea80a99fbdaa9a174c3097c583102
Registration Details
Taiwan FDA Registration: 2eaea80a99fbdaa9a174c3097c583102
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Device Details

"NIHON KOHDEN" Video Intubation Flexible Laryngoscope (Non-sterile)
TW: "ๆ—ฅๆœฌๅ…‰้›ป" ้›ปๅญๅฝฑๅƒๅ–‰้ ญ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2eaea80a99fbdaa9a174c3097c583102

Ministry of Health Medical Device Import No. 020493

DHA09402049308

Company Information

Japan

Product Details

Limited to the first level of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.

D Devices for anesthesiology

D5530 Flexible laryngoscope

Imported from abroad

Dates and Status

May 28, 2019

May 28, 2024