Pure Global

"Armambi" electric blood bag pipe rush blood forceps (unsterilized) - Taiwan Registration 0e6e636214f468044a2aabfe5a42ce8a

Access comprehensive regulatory information for "Armambi" electric blood bag pipe 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 0e6e636214f468044a2aabfe5a42ce8a 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
0e6e636214f468044a2aabfe5a42ce8a
Registration Details
Taiwan FDA Registration: 0e6e636214f468044a2aabfe5a42ce8a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Armambi" electric blood bag pipe rush blood forceps (unsterilized)
TW: โ€œ่‰พ็›Ÿๆฏ”โ€้›ปๅ‹•่ก€่ข‹็ฎก่ทฏ่ถ•่ก€้‰—๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

0e6e636214f468044a2aabfe5a42ce8a

DHA04400894602

Company Information

Germany

Product Details

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

B Hematology, pathology, and genetics

Input;; QMS/QSD

Dates and Status

Jun 28, 2010

Jun 28, 2015

Aug 09, 2018

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€