Qualitative DNA Test Kit for Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma urealyticum, Ureaplasma parvum and Trichomonas vaginalis
Vietnam·Risk Class TTBYT Loại C·Anyplex™ II STI-7e Detection·Seegene, Inc.·Registered Feb 04, 2024- Analysis ID
- 2400209ĐKLH/BYT-HTTB
- Submission ID
- 000.00.04.G18-211012-0004
- Product Type
- Anyplex™ II STI-7e Detection
- Product Code
- SD7701X
- Manufacturer
- Seegene, Inc.
- Manufacturer Country
- REPUBLIC OF
- Authorized Representative
- CÔNG TY TNHH THIẾT BỊ Y TẾ PHƯƠNG ĐÔNG
- Intended Use
- 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.
- Registration Date
- Feb 04, 2024
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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