Pure Global

Nipro GM-30 Inflation Device - Taiwan Registration 4157cdf61650c1c1465d1753f7e98a58

Access comprehensive regulatory information for Nipro GM-30 Inflation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4157cdf61650c1c1465d1753f7e98a58 and manufactured by GOODMAN CO., LTD. GOODMAN RESEARCH CENTER. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..

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
4157cdf61650c1c1465d1753f7e98a58
Registration Details
Taiwan FDA Registration: 4157cdf61650c1c1465d1753f7e98a58
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Nipro GM-30 Inflation Device
TW: ๅฐผๆ™ฎๆด›ๅŸบๆ›ผๆ“ดๅผต่ฃ็ฝฎ
Risk Class 2
MD

Registration Details

4157cdf61650c1c1465d1753f7e98a58

Ministry of Health Medical Device Import No. 034348

DHA05603434805

Company Information

Product Details

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

E Cardiovascular devices

E1650 Vascular photography syringes and syringes

Imported from abroad

Dates and Status

Mar 04, 2021

Mar 04, 2026