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"Fresson" Grysoe Electronic Imaging Laryngoscopy System (Sterilization) - Taiwan Registration 77a11a8c0c5b8679980495d771db6c92

Access comprehensive regulatory information for "Fresson" Grysoe Electronic Imaging Laryngoscopy System (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77a11a8c0c5b8679980495d771db6c92 and manufactured by VERATHON MEDICAL (CANADA) ULC. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..

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77a11a8c0c5b8679980495d771db6c92
Registration Details
Taiwan FDA Registration: 77a11a8c0c5b8679980495d771db6c92
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Device Details

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

Registration Details

77a11a8c0c5b8679980495d771db6c92

DHA04400715202

Company Information

Product Details

Limited to the first level of identification range of "rigid laryngoscopy (D.5540)" and "endotracheal probe (D.5790)" under the Measures for the Administration of Medical Devices.

D Anesthesiology

D.5540 ็กฌๅผๅ–‰้ ญ้ก;; D.5790 ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡

Input;; QMS/QSD

Dates and Status

Oct 21, 2008

Oct 21, 2013

Jan 09, 2017

Cancellation Information

Logged out

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