Ｂ型肝炎核心抗原之抗體檢驗試劑（酵素免疫法）

국가: 대만

언어: 중국어

출처: 衛生福利部食品藥物管理署 (Ministry of Health and Welfare, Food And Drug Administration)

유효 성분:

HEPATITIS B, ANTIGEN, CORE;;HEPATITIS B, ANTIBODY, CORE, PEROXIDASE;;SERUM, ANTI-HBC;;SERUM, HUMAN NORMAL;;HYDROGEN PEROXIDE;;O-PHENYLENEDIAMINE 2HCL (OPD);;SULFURIC ACID (EQ TO SULPHURIC ACID)

제공처:

臺灣安萬特藥品股份有限公司 台北巿松山區復興北路337號12、13、14樓 (97168356)

약제 형태:

試劑

구성:

SULFURIC ACID (EQ TO SULPHURIC ACID) (4036000400) (0.5N); HYDROGEN PEROXIDE (5204900500) 0.3G/L; HEPATITIS B, ANTIGEN, CORE (8081212000) ; HEPATITIS B, ANTIBODY, CORE, PEROXIDASE (8081222200) ; SERUM, HUMAN NORMAL (8082000100) ; SERUM, ANTI-HBC (8082001200) ; O-PHENYLENEDIAMINE 2HCL (OPD) (8084000100)

패키지 단위:

組

수업:

試劑體外用

처방전 유형:

由醫師或檢驗師使用

Manufactured by:

CENTEON PHARMA GMBH. KRUMMBOGEN 10, 35039 MARBURG GERMANYBRUNINGSRASSE 50,D-65926 FRANKFURT AM MAIN ,GERMANY DE

치료 징후:

酵素免疫法測定Ｂ型肝炎核心抗原

제품 요약:

註銷日期: 2006/08/23; 註銷理由: 有效期限已屆; 有效日期: 1999/04/24; 英文品名: ENZYGONST (R) ANTI-HBC (ENZYME IMMUNOASSAY FOR DETERMINATION OF ANTIBODIES TO HE

승인 상태:

已註銷

승인 날짜:

1987-04-24