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"Philips" maternity room information management system - Taiwan Registration a07e8cc502e6ec87778bffd14dd3ab8b

Access comprehensive regulatory information for "Philips" maternity room information management system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a07e8cc502e6ec87778bffd14dd3ab8b 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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a07e8cc502e6ec87778bffd14dd3ab8b
Registration Details
Taiwan FDA Registration: a07e8cc502e6ec87778bffd14dd3ab8b
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Device Details

"Philips" maternity room information management system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ ็”ขๆˆฟ่ณ‡่จŠ็ฎก็†็ณป็ตฑ
Risk Class 2

Registration Details

a07e8cc502e6ec87778bffd14dd3ab8b

DHA05603694201

Company Information

Product Details

Details are as detailed as approved Chinese instructions

l Obstetrics and Gynecology

L.2740 Pre- and post-production monitoring systems and accessories

import

Dates and Status

Mar 16, 2024

Mar 16, 2029