Pure Global

Teleflex airway connector (unsterilized) - Taiwan Registration 67e722e95a0134a38ad63c3ec04f9600

Access comprehensive regulatory information for Teleflex airway connector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67e722e95a0134a38ad63c3ec04f9600 and manufactured by TELEFLEX MEDICAL. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

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
67e722e95a0134a38ad63c3ec04f9600
Registration Details
Taiwan FDA Registration: 67e722e95a0134a38ad63c3ec04f9600
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Teleflex airway connector (unsterilized)
TW: "ๆณฐๅˆฉ็ฆ" ๆฐฃ้“้€ฃๆŽฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

67e722e95a0134a38ad63c3ec04f9600

DHA04401039407

Company Information

Mexico

Product Details

Limited to the first level identification range of the "Airway Connector (D.5810)" of the Measures for the Administration of Medical Devices.

D Anesthesiology

D.5810 Airway connectors

import

Dates and Status

May 24, 2011

May 24, 2021

Nov 08, 2018

Cancellation Information

Logged out

่‡ช่ซ‹่จป้Šท