Taiwan FDA registration 29aa0d499bc79eeb554843adc0e5f2c8

"Ninoon" Chicago self-cleaning suction head (sterilized)

TW: "尼諾恩" 芝加哥自清式抽吸頭(滅菌)

Taiwan·Risk Class 1·GMI Corporation;; NEURO ENTERPRISES, LLC·Registered Nov 07, 2022 – Nov 07, 2027Active

Registration details

Analysis ID: 29aa0d499bc79eeb554843adc0e5f2c8
Customs Code: DHA09402294300

Company information

Manufacturer: GMI Corporation;; NEURO ENTERPRISES, LLC
Manufacturer Country: United States
Authorized Representative: MENEY CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: QMS/QSD;; 委託製造;; 輸入

Dates and status

Registration Date: Nov 07, 2022
Expiry Date: Nov 07, 2027

About this record

Access comprehensive regulatory information for "Ninoon" Chicago self-cleaning suction head (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 29aa0d499bc79eeb554843adc0e5f2c8 and manufactured by GMI Corporation;; NEURO ENTERPRISES, LLC. The authorized representative in Taiwan is MENEY CO., LTD..

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