Pure Global

"PRESSURE PRODUCTS" Hemostatic Pressure Device (Non-Sterile) - Taiwan Registration 7a5c65caf594270f9f5c03b5ead56c5b

Access comprehensive regulatory information for "PRESSURE PRODUCTS" Hemostatic Pressure Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7a5c65caf594270f9f5c03b5ead56c5b and manufactured by PRESSURE PRODUCTS, INC.. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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
7a5c65caf594270f9f5c03b5ead56c5b
Registration Details
Taiwan FDA Registration: 7a5c65caf594270f9f5c03b5ead56c5b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"PRESSURE PRODUCTS" Hemostatic Pressure Device (Non-Sterile)
TW: "ๆ™ฎ้ณไผ‘ๆ™ฎ้”" ๅŠ ๅฃ“ๆญข่ก€ๅธถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

7a5c65caf594270f9f5c03b5ead56c5b

Ministry of Health Medical Device Import No. 021543

DHA09402154302

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".

I General and plastic surgical devices

I5900 Non-inflatable tourniquet

Imported from abroad

Dates and Status

May 15, 2020

May 15, 2025