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Philips Neopap System - Taiwan Registration 8211476e4f68dba424846a3b7d46032f

Access comprehensive regulatory information for Philips Neopap System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8211476e4f68dba424846a3b7d46032f and manufactured by CHILDREN'S MEDICAL VENTURES. 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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8211476e4f68dba424846a3b7d46032f
Registration Details
Taiwan FDA Registration: 8211476e4f68dba424846a3b7d46032f
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Device Details

Philips Neopap System
TW: ้ฃ›ๅˆฉๆตฆๅฐผๆญๆ–ฐ็”Ÿๅ…’ๅ‘ผๅธๅ™จ
Risk Class 2
MD
Cancelled

Registration Details

8211476e4f68dba424846a3b7d46032f

Ministry of Health Medical Device Import No. 025795

DHA05602579503

Company Information

United States

Product Details

D Devices for anesthesiology

D5905 Discontinuous respirators

Imported from abroad

Dates and Status

Jan 17, 2014

Jan 17, 2019

Jul 15, 2022

Cancellation Information

Logged out

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