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"Medtronic" One Press Serter - Taiwan Registration 0f8e7f0d65fc12265ddcf976f9f2f050

Access comprehensive regulatory information for "Medtronic" One Press Serter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f8e7f0d65fc12265ddcf976f9f2f050 and manufactured by MEDTRONIC MINIMED. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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0f8e7f0d65fc12265ddcf976f9f2f050
Registration Details
Taiwan FDA Registration: 0f8e7f0d65fc12265ddcf976f9f2f050
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Device Details

"Medtronic" One Press Serter
TW: "็พŽๆ•ฆๅŠ›" ไธ€ๆŒ‰ๅผ่ผ”ๅŠฉๅ™จ
Risk Class 2
MD

Registration Details

0f8e7f0d65fc12265ddcf976f9f2f050

Ministry of Health Medical Device Import No. 032127

DHA05603212705

Company Information

United States

Product Details

This product is used to assist in the insertion of the "Medtronic" Inlet blood glucose sensor (Weibe Medical Device No. 027206). This product is suitable for a single patient and is not suitable for multiple patients.

A Clinical chemistry and clinical toxicology

A1345 Glucose Test System

Imported from abroad

Dates and Status

Jan 17, 2019

Jan 17, 2024