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"Aiychen" adjustable bending guide probe (sterilized) - Taiwan Registration 1b276f6d6cc92b5a723b923b416e7cfc

Access comprehensive regulatory information for "Aiychen" adjustable bending guide probe (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b276f6d6cc92b5a723b923b416e7cfc and manufactured by GMMI SDN BHD. The authorized representative in Taiwan is DAYCARE HEALTH CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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1b276f6d6cc92b5a723b923b416e7cfc
Registration Details
Taiwan FDA Registration: 1b276f6d6cc92b5a723b923b416e7cfc
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Device Details

"Aiychen" adjustable bending guide probe (sterilized)
TW: โ€œ่‰พ็›Š่พฐโ€ ๅฏ่ชฟๅผๅฝŽๆ›ฒๅฐŽๅผ•ๆŽขๆข (ๆป…่Œ)
Risk Class 1

Registration Details

1b276f6d6cc92b5a723b923b416e7cfc

DHA09402280001

Company Information

Malaysia

Product Details

Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.

D Anesthesiology

D.5790 ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡

Input;; QMS/QSD

Dates and Status

May 05, 2022

May 05, 2027