Taiwan FDA registration 1623f4ade1051188977d72af76e0e8df

Immunolinkage analysis of fetal protein enzyme with Changying A

TW: 常盈甲型胎兒蛋白酵素免疫連結分析法

Taiwan·Risk Class 2·DIAGNOSTIC SYSTEMS LABORATORIES, INC.·Registered Mar 27, 2006 – Mar 27, 2011Cancelled

Registration details

Analysis ID: 1623f4ade1051188977d72af76e0e8df
Customs Code: DHA00601622102

Company information

Manufacturer: DIAGNOSTIC SYSTEMS LABORATORIES, INC.
Manufacturer Country: United States
Authorized Representative: WOLCH ENTERPRISES INC.

Product details

Intended Use: Provides quantitative measurement of AFP in serum.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.6010 腫瘤相關抗原免疫試驗系統
Import Information: import

Dates and status

Registration Date: Mar 27, 2006
Expiry Date: Mar 27, 2011
Cancellation Date: Nov 26, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Immunolinkage analysis of fetal protein enzyme with Changying A in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1623f4ade1051188977d72af76e0e8df and manufactured by DIAGNOSTIC SYSTEMS LABORATORIES, INC.. The authorized representative in Taiwan is WOLCH ENTERPRISES INC..

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