Qualitative DNA Test Kit for Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma urealyticum, Ureaplasma parvum and Trichomonas vaginalis - Vietnam Registration 2400209ĐKLH/BYT-HTTB
Access comprehensive regulatory information for Qualitative DNA Test Kit for Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma urealyticum, Ureaplasma parvum and Trichomonas vaginalis in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại C medical device is registered under number 2400209ĐKLH/BYT-HTTB and manufactured by Seegene, Inc.. The authorized representative in Vietnam is CÔNG TY TNHH THIẾT BỊ Y TẾ PHƯƠNG ĐÔNG.
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Device Details
Registration Details
2400209ĐKLH/BYT-HTTB
000.00.04.G18-211012-0004
Anyplex™ II STI-7e Detection
SD7701X
Technical Details
Qualitative in vitro testing to detect Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma urealyticum, Ureaplasma parvum and Trichomonas vaginalis from urine samples, swabs (urethral, vaginal and cervical) and cell culture samples in liquid.
Dates and Status
Feb 04, 2024

