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"Philips" Central Monitoring Station software - Taiwan Registration 505de69445e5663e26a8955b1ffe04e9

Access comprehensive regulatory information for "Philips" Central Monitoring Station software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 505de69445e5663e26a8955b1ffe04e9 and manufactured by Philips Medizin Systeme Bรถblingen GmbH;; Philips North America LLC. The authorized representative in Taiwan is PHILIPS 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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505de69445e5663e26a8955b1ffe04e9
Registration Details
Taiwan FDA Registration: 505de69445e5663e26a8955b1ffe04e9
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Device Details

"Philips" Central Monitoring Station software
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ ไธญๅคฎ็›ฃ่ฆ–็ซ™่ปŸ้ซ”
Risk Class 2

Registration Details

505de69445e5663e26a8955b1ffe04e9

DHA05603695204

Company Information

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

Mar 29, 2024

Mar 29, 2029