Taiwan FDA registration 30441c1295ffa3b10de205619992e9d3

Bioling Influenza A/B Rapid Test Set

TW: 百歐靈 A/B 型流感快速檢驗試劑組

Taiwan·Risk Class 1·BIOLAND·Registered Oct 28, 2009 – Oct 28, 2014Cancelled

Registration details

Analysis ID: 30441c1295ffa3b10de205619992e9d3
Customs Code: DHA04400824103

Company information

Manufacturer: BIOLAND
Manufacturer Country: Korea, Republic of
Authorized Representative: PAN EXPAND HEALTH CARE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3330 流感病毒血清試劑
Import Information: import

Dates and status

Registration Date: Oct 28, 2009
Expiry Date: Oct 28, 2014
Cancellation Date: Jun 08, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Bioling Influenza A/B Rapid Test Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 30441c1295ffa3b10de205619992e9d3 and manufactured by BIOLAND. The authorized representative in Taiwan is PAN EXPAND HEALTH CARE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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.