Taiwan FDA registration 7468cfc0f4938378cbfaec254f03eadc

"DFI" Diet Check (Non-Sterile)

TW: "敵飛易" 脂肪代謝檢測試劑 (未滅菌)

Taiwan·Risk Class 1·MD·DFI CO.,LTD·Registered Jul 04, 2019 – Jul 04, 2024Expired

Registration details

Analysis ID: 7468cfc0f4938378cbfaec254f03eadc
License Form: Ministry of Health Medical Device Import No. 020622
Customs Code: DHA09402062206

Company information

Manufacturer: DFI CO.,LTD
Manufacturer Country: Korea, Republic of
Authorized Representative: JEHOVAH-JIREH ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "Ketone (Non-quantitative) Test System (A.1435)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1435 Ketone (non-quantitative) test system
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 04, 2019
Expiry Date: Jul 04, 2024

About this record

Access comprehensive regulatory information for "DFI" Diet Check (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7468cfc0f4938378cbfaec254f03eadc and manufactured by DFI CO.,LTD. The authorized representative in Taiwan is JEHOVAH-JIREH ENTERPRISE CO., LTD..

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