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"Kawasumi" blood bag pipe rush blood forceps (unsterilized) - Taiwan Registration d1fda81ee2340b5e8ab8c15f066cebd3

Access comprehensive regulatory information for "Kawasumi" 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 d1fda81ee2340b5e8ab8c15f066cebd3 and manufactured by LMB TECHNOLOGIE GMBH. The authorized representative in Taiwan is K2 INTERNATIONAL 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.

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d1fda81ee2340b5e8ab8c15f066cebd3
Registration Details
Taiwan FDA Registration: d1fda81ee2340b5e8ab8c15f066cebd3
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Device Details

"Kawasumi" blood bag pipe rush blood forceps (unsterilized)
TW: "ๅทๆพ„" ่ก€่ข‹็ฎก่ทฏ่ถ•่ก€้‰— (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d1fda81ee2340b5e8ab8c15f066cebd3

DHA09401686300

Company Information

Germany

Product Details

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

B Hematology, pathology, and genetics

B.9999 Miscellaneous

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Aug 04, 2016

Aug 04, 2021

Sep 19, 2023

Cancellation Information

Logged out

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