Taiwan FDA registration 5bf61dfb04073971b7f31a72ae70727a

"Positive Precision" Bourdon Flowmeter (Unsterilized)

TW: "正氧精密" Bourdon流量計 (未滅菌)

Taiwan·Risk Class 1·Oxygen Precision Technology Co., Ltd. Tainan Factory·Registered Nov 17, 2016 – Nov 17, 2026Active

Registration details

Analysis ID: 5bf61dfb04073971b7f31a72ae70727a

Company information

Manufacturer: Oxygen Precision Technology Co., Ltd. Tainan Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Oxygen Precision Technology Co., Ltd. Tainan Factory

Product details

Intended Use: It is limited to the first level identification scope of the Bourdon Flowmeter (D.2300), which is a classification and grading management method for medical devices.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.2300 Bumblebee流量計
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: Nov 17, 2016
Expiry Date: Nov 17, 2026

About this record

Access comprehensive regulatory information for "Positive Precision" Bourdon Flowmeter (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5bf61dfb04073971b7f31a72ae70727a and manufactured by Oxygen Precision Technology Co., Ltd. Tainan Factory. The authorized representative in Taiwan is Oxygen Precision Technology Co., Ltd. Tainan Factory.

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