Pure Global

"Philips" electrocardiograph - Taiwan Registration 340a7ccc521613d8550a6788da449cae

Access comprehensive regulatory information for "Philips" electrocardiograph in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 340a7ccc521613d8550a6788da449cae and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Philips Medizin Systeme Bรถblingen GmbH;; Philips North America LLC, ;; Philips Goldway (Shenzhen) Industrial Inc., and 2 recent registrations in the same category. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
2 Competitors
2 Recent Registrations
340a7ccc521613d8550a6788da449cae
Registration Details
Taiwan FDA Registration: 340a7ccc521613d8550a6788da449cae
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Philips" electrocardiograph
TW: "้ฃ›ๅˆฉๆตฆ"ๅฟƒ้›ปๅœ–ๅ„€
Risk Class 2
Cancelled

Registration Details

340a7ccc521613d8550a6788da449cae

DHA00601199505

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.2340 Telecardiogram

import

Dates and Status

Sep 23, 2005

Sep 23, 2020

Jul 15, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€