Pure Global

"Denos" multi-channel adapter - Taiwan Registration 5dbe4d218341cf29bf4008863ee73c18

Access comprehensive regulatory information for "Denos" multi-channel adapter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5dbe4d218341cf29bf4008863ee73c18 and manufactured by DIROS TECHNOLOGY INC. The authorized representative in Taiwan is BARRY TEC ENTERPRISE 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
5dbe4d218341cf29bf4008863ee73c18
Registration Details
Taiwan FDA Registration: 5dbe4d218341cf29bf4008863ee73c18
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Denos" multi-channel adapter
TW: โ€œๆˆด่ซพๆ–ฏโ€ๅคš้ ป้“่ฝ‰ๆŽฅๅ™จ
Risk Class 2

Registration Details

5dbe4d218341cf29bf4008863ee73c18

DHA00602301003

Company Information

Canada

Product Details

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

K Neuroscience

K.4400 Shot Cutout Generator

import

Dates and Status

Nov 11, 2011

Nov 11, 2026