Taiwan FDA registration 4d29bb82f39c64240264db33a4604201

"EULOGIUMS" PENTAX Video Intubation Flexible Laryngoscope (Non-Sterile)

TW: "裕強" 賓得士電子影像喉頭鏡 (未滅菌)

Taiwan·Risk Class 1·MD·Xinghe Biomedical Co., Ltd. Taichung Factory·Registered Oct 11, 2017 – Oct 11, 2022Cancelled

Registration details

Analysis ID: 4d29bb82f39c64240264db33a4604201
License Form: Ministry of Health Medical Device Manufacturing No. 006966

Company information

Manufacturer: Xinghe Biomedical Co., Ltd. Taichung Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: EULOGIUMS CO., LTD.

Product details

Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5530 Flexible laryngoscope
Import Information: Produced in Taiwan, China; Contract manufacturing

Dates and status

Registration Date: Oct 11, 2017
Expiry Date: Oct 11, 2022
Cancellation Date: Aug 06, 2018

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "EULOGIUMS" PENTAX 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 4d29bb82f39c64240264db33a4604201 and manufactured by Xinghe Biomedical Co., Ltd. Taichung Factory. The authorized representative in Taiwan is EULOGIUMS CO., LTD..

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