Pure Global

"Schiller" Magraft standard physiological monitoring equipment - Taiwan Registration 5d87a9d5529119717b87f94979aefd83

Access comprehensive regulatory information for "Schiller" Magraft standard physiological monitoring equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5d87a9d5529119717b87f94979aefd83 and manufactured by SCHILLER MEDICAL. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
5d87a9d5529119717b87f94979aefd83
Registration Details
Taiwan FDA Registration: 5d87a9d5529119717b87f94979aefd83
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Schiller" Magraft standard physiological monitoring equipment
TW: โ€œๅธญๅ‹’โ€็พŽๆ ผ่ŠๅฏŒๆจ™ๆบ–ๅž‹็”Ÿ็†็›ฃ่ฆ–่จญๅ‚™
Risk Class 2
Cancelled

Registration Details

5d87a9d5529119717b87f94979aefd83

DHA00602117703

Company Information

France

Product Details

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

E Cardiovascular Medicine Science

E.2300 Cardiac monitor (including cardiac data and heart rate monitor)

import

Dates and Status

Jun 30, 2010

Jun 30, 2020

May 19, 2022

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ