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"Kirby" Knoss High Level Anesthesia Depth Monitor - Taiwan Registration 7088790e7ed86ea4f1ece8a6686f8f5e

Access comprehensive regulatory information for "Kirby" Knoss High Level Anesthesia Depth Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7088790e7ed86ea4f1ece8a6686f8f5e and manufactured by Fresenius Vial S.A.S.;; Fresenius Kabi AG. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.

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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7088790e7ed86ea4f1ece8a6686f8f5e
Registration Details
Taiwan FDA Registration: 7088790e7ed86ea4f1ece8a6686f8f5e
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Device Details

"Kirby" Knoss High Level Anesthesia Depth Monitor
TW: โ€œๅกๆฏ”โ€ๅ…‹่ซพๆ–ฏ้ซ˜้šŽ้บป้†‰ๆทฑๅบฆ็›ฃๆธฌๅ„€
Risk Class 2

Registration Details

7088790e7ed86ea4f1ece8a6686f8f5e

DHA05603718900

Company Information

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

May 31, 2024

May 31, 2029