Taiwan FDA registration 7ea96a35e3813130ecaf39506871b1a1

"Kaijie" Canadian Solar Epstein-Barr Virus Nucleic Acid Test Set (Unsterilized)

TW: "凱杰" 阿特斯 EB病毒核酸檢驗試劑組 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·QIAGEN GMBH·Registered Feb 22, 2013 – Feb 22, 2018Cancelled
Registration details
Analysis ID
7ea96a35e3813130ecaf39506871b1a1
Customs Code
DHA04401273402
Company information
Manufacturer
QIAGEN GMBH
Manufacturer Country
Germany
Authorized Representative
QIAGEN TAIWAN COMPANY LIMITED
Product details
Intended Use
Limited to the first level identification range of "Epstein-Barr virus serum reagent (C.3235)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3235 EB病毒血清試劑
Import Information
import
Dates and status
Registration Date
Feb 22, 2013
Expiry Date
Feb 22, 2018
Cancellation Date
Nov 20, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Kaijie" Canadian Solar Epstein-Barr Virus Nucleic Acid Test Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7ea96a35e3813130ecaf39506871b1a1 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including QIAGEN GMBH, 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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