Taiwan FDA registration a1e340d85ba6e587176a66681e282aad
"Passy Muir" Airway connector (Non-Sterile)
TW: "佩斯米爾" 氣道連接器 (未滅菌)
Registration details
- Analysis ID
- a1e340d85ba6e587176a66681e282aad
- License Form
- Ministry of Health Medical Device Import No. 016554
- Customs Code
- DHA09401655400
Company information
- Manufacturer
- PASSY-MUIR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- RTSYSTEM INC.
Product details
- Intended Use
- Limited to the first level identification range of the "Airway Connector (D.5810)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5810 airway connector
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 19, 2016
- Expiry Date
- May 19, 2021
About this record
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 DatabasePowered by Pure Global AI89,000+ Devices