Taiwan FDA registration 89c89e7bbe69b2e8709c0a640b2bf8c2
“Serim” PyloriTek Test Kit(Non-Sterile)
TW: “偲靈”幽門桿菌測試組(未滅菌)
Taiwan·Risk Class 1·MD·Serim Research Corporation·Registered Nov 06, 2018 – Nov 06, 2023ExpiredRegistration details
- Analysis ID
- 89c89e7bbe69b2e8709c0a640b2bf8c2
- License Form
- Ministry of Health Medical Device Import No. 019784
- Customs Code
- DHA09401978406
Company information
- Manufacturer
- Serim Research Corporation
- Manufacturer Country
- United States
- Authorized Representative
- TEN QUIN MEDICAL SUPPLY 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 06, 2018
- Expiry Date
- Nov 06, 2023
About this record
Access comprehensive regulatory information for “Serim” PyloriTek Test Kit(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 89c89e7bbe69b2e8709c0a640b2bf8c2 and manufactured by Serim Research Corporation. The authorized representative in Taiwan is TEN QUIN MEDICAL SUPPLY CO., LTD..
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