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"Fresson" Glaiser Electronic Imaging Laryngoscopy System (Sterile/Unsterile) - Taiwan Registration 6df9433025ae4d46262ff7ee3f07f58e

Access comprehensive regulatory information for "Fresson" Glaiser Electronic Imaging Laryngoscopy System (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6df9433025ae4d46262ff7ee3f07f58e and manufactured by VERATHON MEDICAL (CANADA) ULC. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..

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6df9433025ae4d46262ff7ee3f07f58e
Registration Details
Taiwan FDA Registration: 6df9433025ae4d46262ff7ee3f07f58e
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Device Details

"Fresson" Glaiser Electronic Imaging Laryngoscopy System (Sterile/Unsterile)
TW: โ€œๆ–็‘ž้ Œโ€ๆ ผ่Š็ดข้›ปๅญๅฝฑๅƒๅ–‰้ ญ้ก็ณป็ตฑ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

6df9433025ae4d46262ff7ee3f07f58e

DHA04401164001

Company Information

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

Input;; QMS/QSD

Dates and Status

Apr 30, 2012

Apr 30, 2027