Pure Global

"Passy Muir" Airway connector (Non-Sterile) - Taiwan Registration a1e340d85ba6e587176a66681e282aad

Access comprehensive regulatory information for "Passy Muir" Airway connector (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a1e340d85ba6e587176a66681e282aad and manufactured by PASSY-MUIR, INC.. The authorized representative in Taiwan is RTSYSTEM 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
a1e340d85ba6e587176a66681e282aad
Registration Details
Taiwan FDA Registration: a1e340d85ba6e587176a66681e282aad
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Passy Muir" Airway connector (Non-Sterile)
TW: "ไฝฉๆ–ฏ็ฑณ็ˆพ" ๆฐฃ้“้€ฃๆŽฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a1e340d85ba6e587176a66681e282aad

Ministry of Health Medical Device Import No. 016554

DHA09401655400

Company Information

United States

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 Devices for anesthesiology

D5810 airway connector

Imported from abroad

Dates and Status

May 19, 2016

May 19, 2021