Taiwan FDA registration b75d2330f6baac1931e5299e37df815c

"Pervice" Lymphocyte separation medium (Non-Sterile)

TW: “必為西”淋巴球分離培養基 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·PERVICE KOREA CO., LTD.·Registered Nov 04, 2019 – Nov 04, 2024Expired
Registration details
Analysis ID
b75d2330f6baac1931e5299e37df815c
License Form
Ministry of Health Medical Device Import No. 021004
Customs Code
DHA09402100401
Company information
Manufacturer Country
Korea, Republic of
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Lymphocyte Separation Medium (B.8500)".
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B8500 Lymphocyte Isolation Medium
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 04, 2019
Expiry Date
Nov 04, 2024
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About this record

Access comprehensive regulatory information for "Pervice" Lymphocyte separation medium (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 b75d2330f6baac1931e5299e37df815c and manufactured by PERVICE KOREA CO., LTD.. The authorized representative in Taiwan is Shiang Tai Medical Instructment CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PERVICE KOREA CO., LTD., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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