Taiwan FDA registration a283afc81addea1c008de2f33c1cf05e

"Fama" Hanmini Heat and Moisture Condenser (Artificial Nose) (Unsterilized)

TW: “法瑪”漢米尼熱及濕氣凝結器(人工鼻)(未滅菌)
Taiwan flagTaiwan·Risk Class 1·PHARMA SYSTEMS AB·Registered Jan 03, 2008 – Jan 03, 2013Cancelled
Registration details
Analysis ID
a283afc81addea1c008de2f33c1cf05e
Customs Code
DHA04400643802
Company information
Manufacturer
PHARMA SYSTEMS AB
Manufacturer Country
Sweden
Authorized Representative
BIOSYSTEMS INC.
Product details
Intended Use
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Heat and Moisture Condenser (Artificial Nose) (D.5375)".
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5375 Heat and humidity condenser (artificial nose)
Import Information
import
Dates and status
Registration Date
Jan 03, 2008
Expiry Date
Jan 03, 2013
Cancellation Date
Jun 11, 2015
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Fama" Hanmini Heat and Moisture Condenser (Artificial Nose) (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a283afc81addea1c008de2f33c1cf05e and manufactured by PHARMA SYSTEMS AB. The authorized representative in Taiwan is BIOSYSTEMS 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