Taiwan FDA registration 0330e94f1314e9dd89c610e489367c50

"Bard" urethral dilator attachment (unsterilized)

TW: “巴德”尿道擴張器附件 (未滅菌)

Taiwan·Risk Class 1·C.R. BARD, INC.·Registered Jan 08, 2010 – Jan 08, 2015Cancelled

Registration details

Analysis ID: 0330e94f1314e9dd89c610e489367c50
Customs Code: DHA04400825300

Company information

Manufacturer: C.R. BARD, INC.
Manufacturer Country: United States
Authorized Representative: BARD PACIFIC HEALTH CARE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of "urethral dilator (H.5520)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.5520 Urethral extender
Import Information: import

Dates and status

Registration Date: Jan 08, 2010
Expiry Date: Jan 08, 2015
Cancellation Date: May 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Bard" urethral dilator attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0330e94f1314e9dd89c610e489367c50 and manufactured by C.R. BARD, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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