Taiwan FDA registration dc26eda83418c8a70384dbad37e0e13d

"Bard" urethral spies (unsterilized)

TW: “巴德”尿道探子（未滅菌）

Taiwan·Risk Class 1·C.R. BARD, INC.·Registered Nov 24, 2009 – Nov 24, 2014Cancelled

Registration details

Analysis ID: dc26eda83418c8a70384dbad37e0e13d
Customs Code: DHA04400831506

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: Nov 24, 2009
Expiry Date: Nov 24, 2014
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 spies (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dc26eda83418c8a70384dbad37e0e13d and manufactured by C.R. BARD, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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