Pure Global

"Pajik" balloon cannula set - Taiwan Registration 081bf8c10265cfc0c4e943643bada610

Access comprehensive regulatory information for "Pajik" balloon cannula set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 081bf8c10265cfc0c4e943643bada610 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong 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
081bf8c10265cfc0c4e943643bada610
Registration Details
Taiwan FDA Registration: 081bf8c10265cfc0c4e943643bada610
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Pajik" balloon cannula set
TW: โ€œๅธ•ๅฐ‡ๅ…‹โ€็ƒๅ›Šๅฅ—็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

081bf8c10265cfc0c4e943643bada610

DHA00602043102

Company Information

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Nov 24, 2009

Nov 24, 2019

Aug 05, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€