Taiwan FDA registration 6bd2380251d2225fa788ac9cd409fa07

"E-TAKE" Helicobacter Pylori Reagents (Non-sterile)

TW: "醫達" 幽門桿菌試劑 (未滅菌)

Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered Nov 21, 2017 – Nov 21, 2022Expired

Registration details

Analysis ID: 6bd2380251d2225fa788ac9cd409fa07
License Form: Ministry of Health Medical Device Import No. 018528
Customs Code: DHA09401852809

Company information

Manufacturer: MD BIOTECH CORPORATION
Manufacturer Country: United States
Authorized Representative: E-TAKE TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C0003 Helicobacter serological reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 21, 2017
Expiry Date: Nov 21, 2022

About this record

Access comprehensive regulatory information for "E-TAKE" Helicobacter Pylori Reagents (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 6bd2380251d2225fa788ac9cd409fa07 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is E-TAKE TECHNOLOGY CO., LTD..

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