Pure Global

"Hao Kensheng" vascular diagnostic instrument - Taiwan Registration a5d851dde30df06b5e8af778dbeed592

Access comprehensive regulatory information for "Hao Kensheng" vascular diagnostic instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a5d851dde30df06b5e8af778dbeed592 and manufactured by D.E. HOKANSON INC.. The authorized representative in Taiwan is NIEN TAI MEDICAL INSTRUMENTS CO., LTD..

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
a5d851dde30df06b5e8af778dbeed592
Registration Details
Taiwan FDA Registration: a5d851dde30df06b5e8af778dbeed592
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Hao Kensheng" vascular diagnostic instrument
TW: "ๅฅฝ่‚ฏ็”Ÿ" ่ก€็ฎก่จบๆ–ทๅ„€
Risk Class 2
Cancelled

Registration Details

a5d851dde30df06b5e8af778dbeed592

DHA00601191303

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Sep 13, 2005

Sep 13, 2015

Apr 25, 2018

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ