Taiwan FDA registration 7819c468127d7404f0c3ad31278b5e8a

"Hongji" disposable flexible imaging ureteral nephroscopy

TW: “宏濟”一次性軟式影像輸尿管腎鏡

Taiwan·Risk Class 2·Shenzhen HugeMed Medical Technical Development Co., Ltd.·Registered Aug 18, 2022 – Aug 18, 2027Active

Registration details

Analysis ID: 7819c468127d7404f0c3ad31278b5e8a
Customs Code: DHA09200137505

Company information

Manufacturer: Shenzhen HugeMed Medical Technical Development Co., Ltd.
Manufacturer Country: China
Authorized Representative: Kang Cheng Medical Technology Co., Ltd

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: Chinese goods;; input

Dates and status

Registration Date: Aug 18, 2022
Expiry Date: Aug 18, 2027

About this record

Access comprehensive regulatory information for "Hongji" disposable flexible imaging ureteral nephroscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7819c468127d7404f0c3ad31278b5e8a and manufactured by Shenzhen HugeMed Medical Technical Development Co., Ltd.. The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.

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