Taiwan FDA registration 65dc1b807bfefb0c19eab941fe9c3749

"Xiamen" Dingjing blood collection pen (unsterilized)

TW: "廈門"鼎晶採血筆(未滅菌)

Taiwan·Risk Class 1·NIPRO DIAGNOSTICS, INC.;; XIAMEN DINGJING PLASTIC CO., LTD.·Registered Mar 24, 2011 – Mar 24, 2016Cancelled

Registration details

Analysis ID: 65dc1b807bfefb0c19eab941fe9c3749
Customs Code: DHA04600131105

Company information

Manufacturer: NIPRO DIAGNOSTICS, INC.;; XIAMEN DINGJING PLASTIC CO., LTD.
Manufacturer Country: United States;;China
Authorized Representative: Taiwan Nipro Medical Device Co., Ltd

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: Contract manufacturing;; input

Dates and status

Registration Date: Mar 24, 2011
Expiry Date: Mar 24, 2016
Cancellation Date: May 10, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Xiamen" Dingjing blood collection pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 65dc1b807bfefb0c19eab941fe9c3749 and manufactured by NIPRO DIAGNOSTICS, INC.;; XIAMEN DINGJING PLASTIC CO., LTD.. The authorized representative in Taiwan is Taiwan Nipro Medical Device Co., Ltd.

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