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“Philips” IntelliSpare Perinatal - Taiwan Registration 7f8f6e20b406dd593fcd22bcf4968310

Access comprehensive regulatory information for “Philips” IntelliSpare Perinatal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f8f6e20b406dd593fcd22bcf4968310 and manufactured by PHILIPS MEDICAL SYSTEMS. 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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7f8f6e20b406dd593fcd22bcf4968310
Registration Details
Taiwan FDA Registration: 7f8f6e20b406dd593fcd22bcf4968310
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Device Details

“Philips” IntelliSpare Perinatal
TW: “飛利浦”產房資訊管理系統
Risk Class 2
MD
Cancelled

Registration Details

7f8f6e20b406dd593fcd22bcf4968310

Ministry of Health Medical Device Import No. 025462

DHA05602546202

Company Information

United States

Product Details

l Devices for obstetrics and gynecology

L2740 Pre- and post-production monitoring system and its accessories

Imported from abroad

Dates and Status

Nov 14, 2013

Nov 14, 2018

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者