Taiwan FDA registration 2eaea80a99fbdaa9a174c3097c583102

"NIHON KOHDEN" Video Intubation Flexible Laryngoscope (Non-sterile)

TW: "日本光電" 電子影像喉頭鏡 (未滅菌)

Taiwan·Risk Class 1·MD·NIHON KOHDEN CORPORATION·Registered May 28, 2019 – May 28, 2024Expired

Registration details

Analysis ID: 2eaea80a99fbdaa9a174c3097c583102
License Form: Ministry of Health Medical Device Import No. 020493
Customs Code: DHA09402049308

Company information

Manufacturer: NIHON KOHDEN CORPORATION
Manufacturer Country: Japan
Authorized Representative: PARAMOUNT LAND COMPANY LTD.

Product details

Intended Use: Limited to the first level of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5530 Flexible laryngoscope
Import Information: Imported from abroad

Dates and status

Registration Date: May 28, 2019
Expiry Date: May 28, 2024

About this record

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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