VITROLIFE G-MOPS™ Plus - Indonesia BPOM Medical Device Registration
VITROLIFE G-MOPS™ Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106704864. 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 PT. DIPA PHARMALAB INTERSAINS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VITROLIFE SWEDEN AB.Country of Origin
Sweden
Authorized Representative
PT. DIPA PHARMALAB INTERSAINSAR Address
Jl. Raya Kebayoran Lama No. 28, Kebayoran Lama,Jakarta Selatan, DKl Jakarta, kode pos : 12210
Registration Date
Sep 27, 2024
Expiry Date
Dec 27, 2028
Product Type
Reproductive Aids
Reproductive media and supplements.
Non Electromedic Sterile
VITROLIFE G-1 Plus
RAPIDWARM™ Cleave
G-MOPS™
VITROLIFE HSA-Solution™
ICSI™
EMBRYOGLUE
VITROLIFE Handling Pipette
VITROLIFE HYASE™ - 10X
G-RINSE ™
VITROLIFE SpermFreeze Solution™
VITROLIFE G-1 Plus
VITROLIFE SWEDEN AB.
IALURIL Prefill
IBSA FARMACEUTICI ITALIA, SRL
RAPIDWARM™ Cleave
VITROLIFE SWEDEN AB.
G-MOPS™
VITROLIFE SWEDEN AB.
EMBRYOGLUE
VITROLIFE SWEDEN AB.
VITROLIFE Centrifuge Tube
VITROLIFE SWEDEN AB
VITROLIFE Pasteur Pipette
VITROLIFE SWEDEN AB
VITROLIFE 5 WELL Culture Dish
VITROLIFE SWEDEN AB
VITROLIFE Micro-Droplet Culture Dish
VITROLIFE SWEDEN AB
VITROLIFE Serological Pipette
VITROLIFE SWEDEN AB

