Pure Global

"Ambi" blood bag line rush blood forceps (unsterilized) - Taiwan Registration 5e4f84010367c2017a1edfaae442fa18

Access comprehensive regulatory information for "Ambi" blood bag line rush blood forceps (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5e4f84010367c2017a1edfaae442fa18 and manufactured by LMB TECHNOLOGIE GMBH. The authorized representative in Taiwan is AMAZING MEDICAL INC..

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
5e4f84010367c2017a1edfaae442fa18
Registration Details
Taiwan FDA Registration: 5e4f84010367c2017a1edfaae442fa18
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Ambi" blood bag line rush blood forceps (unsterilized)
TW: "่‰พ็›Ÿๆฏ”" ่ก€่ข‹็ฎก่ทฏ่ถ•่ก€้‰— (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5e4f84010367c2017a1edfaae442fa18

DHA04400853800

Company Information

Germany

Product Details

Squeeze the residual blood from the blood bag line into the blood bag.

B Hematology, pathology, and genetics

B.9050 Blood bank supply equipment

import

Dates and Status

May 07, 2010

May 07, 2020

Jul 15, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€