Taiwan FDA registration a1c1e51ac31b4bb865a24957f7fdf696

Wudingliano blood collection device (unsterilized)

TW: 五鼎連諾採血器(未滅菌)

Taiwan·Risk Class 1·GLOBAL MEDICAL MARKET CORP.·Registered Apr 09, 2008 – Apr 09, 2018Cancelled

Registration details

Analysis ID: a1c1e51ac31b4bb865a24957f7fdf696
Customs Code: DHA04400665000

Company information

Manufacturer: GLOBAL MEDICAL MARKET CORP.
Manufacturer Country: Korea, Republic of
Authorized Representative: APEX BIOTECHNOLOGY CORPORATION

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Apr 09, 2008
Expiry Date: Apr 09, 2018
Cancellation Date: Dec 20, 2019

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for Wudingliano blood collection device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a1c1e51ac31b4bb865a24957f7fdf696 and manufactured by GLOBAL MEDICAL MARKET CORP.. The authorized representative in Taiwan is APEX BIOTECHNOLOGY CORPORATION.

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