Taiwan FDA registration 09e655401f87d80ad4a6201f3eb57a82

"Fama" heat and moisture condenser (artificial nose)

TW: "法瑪" 熱及濕氣凝結器(人工鼻)
Taiwan flagTaiwan·Risk Class 1·PHARMA SYSTEMS AB·Registered Feb 27, 2006 – Feb 27, 2011Cancelled
Registration details
Analysis ID
09e655401f87d80ad4a6201f3eb57a82
Customs Code
DHA04400274300
Company information
Manufacturer
PHARMA SYSTEMS AB
Manufacturer Country
Sweden
Authorized Representative
BIOSYSTEMS INC.
Product details
Intended Use
A heat and moisture condenser (artificial nose) is a device that is placed on a tracheostomy (surgical opening in the larynx) or endotracheal tube (a tube placed in the trachea) to warm and moisten the breath of the patient.
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
Feb 27, 2006
Expiry Date
Feb 27, 2011
Cancellation Date
Nov 22, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Fama" heat and moisture condenser (artificial nose) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 09e655401f87d80ad4a6201f3eb57a82 and manufactured by PHARMA SYSTEMS AB. The authorized representative in Taiwan is BIOSYSTEMS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHARMA SYSTEMS AB, and 1 recent registrations in the same category. 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.

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