Gx-MOPS ™ PLUS - Indonesia BPOM Medical Device Registration
Gx-MOPS ™ PLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105320118. The device is manufactured by VITROLIFE SWEDEN AB from Sweden, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DIPA PHARMALAB INTERSAINS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VITROLIFE SWEDEN ABCountry of Origin
Sweden
Authorized Representative
DIPA PHARMALAB INTERSAINSAR Address
Jl. Raya Kebayoran Lama No. 28, Kebayoran Lama,Jakarta Selatan, DKl Jakarta, kode pos : 12210
Registration Date
Oct 25, 2023
Expiry Date
Jun 30, 2028
Product Type
Reproductive Aids
Reproductive media and supplements.
Non Electromedic Sterile
VITROLIFE Centrifuge Tube
CULTURE DISH
VITROLIFE Pasteur Pipette
VITROLIFE Collection Dish
ICSI Dish
VITROLIFE Micro-Droplet Culture Dish
VITROLIFE 5 WELL Culture Dish
VITROLIFE Serological Pipette
SAMPLE TUBE
OOCYTE COLLECTION TUBE
VITROLIFE HSA-Solution™
VITROLIFE SWEDEN AB.
ICSI™
VITROLIFE SWEDEN AB.
CULTURE DISH
VITROLIFE SWEDEN AB
PEROSSAL Resorbable Hydroxy Apatite for Filling of Bone Defects
OSARTIS GMBH
IALUSET PLUS Cream
IBSA PHARMA SAS.,
Gx-IVF ™
VITROLIFE SWEDEN AB
Gx-TL ™
VITROLIFE SWEDEN AB
RAPIDVIT™ Cleave
VITROLIFE SWEDEN AB.
SPERMRINSE ™
VITROLIFE SWEDEN AB.
VITROLIFE G-2™ Plus
VITROLIFE SWEDEN AB.