Taiwan FDA registration b35fd700292ff090fbe18456c18a106b

Aiji asthma aid device

TW: 愛治喘噴藥輔助器
Taiwan flagTaiwan·Risk Class 1·MONAGHAN MEDICAL CORP.·Registered Dec 01, 2005 – Dec 01, 2010Cancelled
Registration details
Analysis ID
b35fd700292ff090fbe18456c18a106b
Customs Code
DHA04400217502
Company information
Manufacturer Country
United States
Authorized Representative
STANDARD HEALTH MEDICAL CO., LTD.
Product details
Intended Use
This product needs to be used in conjunction with a metered spray to infuse the drug into the lungs of the intubated patient.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5810 Airway connectors
Import Information
import
Dates and status
Registration Date
Dec 01, 2005
Expiry Date
Dec 01, 2010
Cancellation Date
Nov 16, 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 Aiji asthma aid device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b35fd700292ff090fbe18456c18a106b and manufactured by MONAGHAN MEDICAL CORP.. The authorized representative in Taiwan is STANDARD HEALTH MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MONAGHAN MEDICAL CORP., 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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