Taiwan FDA registration 64014745e3a41ff9be56b397614fd014

"Chaoyang" endoscope defogging (heating) package (sterilization)

TW: “朝揚”內視鏡除霧(加熱)包(滅菌)

Taiwan·Risk Class 1·Chaoyang Plastic Factory Co., Ltd·Registered Feb 23, 2019 – Feb 23, 2029Active

Registration details

Analysis ID: 64014745e3a41ff9be56b397614fd014

Company information

Manufacturer: Chaoyang Plastic Factory Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Chaoyang Plastic Factory Co., Ltd

Product details

Intended Use: Limited to the first level recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Feb 23, 2019
Expiry Date: Feb 23, 2029

About this record

Access comprehensive regulatory information for "Chaoyang" endoscope defogging (heating) package (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 64014745e3a41ff9be56b397614fd014 and manufactured by Chaoyang Plastic Factory Co., Ltd. The authorized representative in Taiwan is Chaoyang Plastic Factory Co., Ltd.

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