Taiwan FDA registration b8ac7e4d327a4fec7f0084dbe52adb56
"Neo-branched" human T-lymphotropic virus antibody Western ink dot method 2.4 reagent
TW: “新科化” 人類嗜T淋巴球病毒抗體西方墨點法2.4試劑
Registration details
- Analysis ID
- b8ac7e4d327a4fec7f0084dbe52adb56
- Customs Code
- DHA00602384808
Company information
- Manufacturer
- MP BIOMEDICALS ASIA PACIFIC PTE. LTD.
- Manufacturer Country
- Singapore
- Authorized Representative
- NEW SCIENTIFIC EQUIPMENT CO., LTD.
Product details
- Intended Use
- Western ink spots are legally tested for T-lymphotropic virus type 1 and type 2 antibodies in human serum or plasma, and are used for confirmation.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4020 Analysis of specific tests
- Import Information
- import
Dates and status
- Registration Date
- Aug 16, 2012
- Expiry Date
- Jun 04, 2014
- Cancellation Date
- May 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Neo-branched" human T-lymphotropic virus antibody Western ink dot method 2.4 reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b8ac7e4d327a4fec7f0084dbe52adb56 and manufactured by MP BIOMEDICALS ASIA PACIFIC PTE. LTD.. The authorized representative in Taiwan is NEW SCIENTIFIC EQUIPMENT CO., LTD..
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