Taiwan FDA registration 78a49399eaef89cbd57db0b2e152f090

Nipro Tianjin Huahong blood collection needle (sterilized)

TW: 尼普洛天津華鴻採血針(滅菌)

Taiwan·Risk Class 1·NIPRO DIAGNOSTICS, INC.;; TIANJIN HUAHONG MEDICAL CO., LTD.·Registered Feb 08, 2011 – Feb 08, 2016Cancelled

Registration details

Analysis ID: 78a49399eaef89cbd57db0b2e152f090
Customs Code: DHA04600128201

Company information

Manufacturer: NIPRO DIAGNOSTICS, INC.;; TIANJIN HUAHONG MEDICAL 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;; Chinese goods;; input

Dates and status

Registration Date: Feb 08, 2011
Expiry Date: Feb 08, 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 Nipro Tianjin Huahong blood collection needle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 78a49399eaef89cbd57db0b2e152f090 and manufactured by NIPRO DIAGNOSTICS, INC.;; TIANJIN HUAHONG MEDICAL CO., LTD.. The authorized representative in Taiwan is Taiwan Nipro Medical Device Co., Ltd.

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