Pure Global

"Fuzhan Mei" respirator tubing (unsterilized) - Taiwan Registration 2a85704e88c87a1eb782459a5ee092b7

Access comprehensive regulatory information for "Fuzhan Mei" 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 2a85704e88c87a1eb782459a5ee092b7 and manufactured by Fuzhan Mei Technology Co., Ltd. Dongshan Factory. The authorized representative in Taiwan is FOXXMED 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
2a85704e88c87a1eb782459a5ee092b7
Registration Details
Taiwan FDA Registration: 2a85704e88c87a1eb782459a5ee092b7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Fuzhan Mei" respirator tubing (unsterilized)
TW: "็ฆๅฑ•็พŽ"ๅ‘ผๅธๅ™จ็ฎก่ทฏ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

2a85704e88c87a1eb782459a5ee092b7

Company Information

Taiwan, Province of China

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

Domestic

Dates and Status

Feb 16, 2015

Feb 16, 2030