Taiwan FDA registration 5fdc916cebe98a3750cc27b5461348fd

Ikang ovulation detection reagent

TW: 艾康排卵檢測試劑

Taiwan·Risk Class 1·ACON BIOTECH (HANGZHOU) CO., LTD.·Registered May 09, 2006 – May 09, 2011Cancelled

Registration details

Analysis ID: 5fdc916cebe98a3750cc27b5461348fd
Customs Code: DHA04600024309

Company information

Manufacturer: ACON BIOTECH (HANGZHOU) CO., LTD.
Manufacturer Country: China
Authorized Representative: GENERAL BIOLOGICALS CORP.

Product details

Intended Use: Limited to the first level of identification range of the Luteinizing Hokin Test System (A.1485) for the Administrative Measures for Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1485 Progesterone testing system
Import Information: import

Dates and status

Registration Date: May 09, 2006
Expiry Date: May 09, 2011
Cancellation Date: Nov 28, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Ikang ovulation detection reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5fdc916cebe98a3750cc27b5461348fd and manufactured by ACON BIOTECH (HANGZHOU) CO., LTD.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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