Pure Global

"Vibim" respirator tubing (unsterilized) - Taiwan Registration edcdcb026ff285ae4f86c870646558bb

Access comprehensive regulatory information for "Vibim" respirator tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number edcdcb026ff285ae4f86c870646558bb and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GRANDMEDICAL ENTERPRISE 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
edcdcb026ff285ae4f86c870646558bb
Registration Details
Taiwan FDA Registration: edcdcb026ff285ae4f86c870646558bb
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Vibim" respirator tubing (unsterilized)
TW: "็ถญๆฏ”ๅง†"ๅ‘ผๅธๅ™จ็ฎก่ทฏ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

edcdcb026ff285ae4f86c870646558bb

DHA09402033503

Company Information

Germany

Product Details

Limited to the first level identification range of the "Respirator Pipeline (D.5975)" of the Measures for the Classification and Grading Management of Medical Equipment.

D Anesthesiology

D.5975 Respirator Tubing

import

Dates and Status

Apr 18, 2019

Apr 18, 2029