Taiwan FDA registration b228d86ed42cb402353b2c129182f1eb

"Cardino" wound drainage device (sterilization)

TW: "卡迪諾" 傷口引流裝置 (滅菌)
Taiwan flagTaiwan·Risk Class 1·CARDINAL HEALTH, INC.·Registered Mar 11, 2011 – Mar 11, 2016Cancelled
Registration details
Analysis ID
b228d86ed42cb402353b2c129182f1eb
Customs Code
DHA04401000203
Company information
Manufacturer Country
United States
Authorized Representative
BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
Intended Use
Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4200 Incoming/Drainage Tubes and Accessories
Import Information
import
Dates and status
Registration Date
Mar 11, 2011
Expiry Date
Mar 11, 2016
Cancellation Date
May 28, 2018
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 "Cardino" wound drainage device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b228d86ed42cb402353b2c129182f1eb and manufactured by CARDINAL HEALTH, INC.. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including CARDINAL HEALTH P.R. 218, INC., CARDINAL HEALTH, INC., and 2 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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