Taiwan FDA registration ea02048348995bcf7289072d48cc4895

"McTay" vacuum wound drainage sleeve (sterilized)

TW: “邁克泰” 真空傷口引流套(滅菌)
Taiwan flagTaiwan·Risk Class 1·MICROTEK DOMINICANA, S.A.·Registered Feb 06, 2006 – Feb 06, 2021Cancelled
Registration details
Analysis ID
ea02048348995bcf7289072d48cc4895
Customs Code
DHA04400258403
Company information
Manufacturer Country
Dominican Republic
Authorized Representative
CHINA HOSMED INTERNATIONAL INC.
Product details
Intended Use
The non-motivated, single-patient-use, portable suction appliance contains a manual plastic, disposable aspiration system for vacuum drainage of surgical wounds.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4680 Non-motive, single patient-use, carry-on suctioning device
Import Information
import
Dates and status
Registration Date
Feb 06, 2006
Expiry Date
Feb 06, 2021
Cancellation Date
Oct 12, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "McTay" vacuum wound drainage sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ea02048348995bcf7289072d48cc4895 and manufactured by MICROTEK DOMINICANA, S.A.. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL 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