SPERMRINSE ™ - Indonesia BPOM Medical Device Registration
SPERMRINSE ™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106110448. 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.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
VITROLIFE SWEDEN AB.Country 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
Aug 04, 2023
Expiry Date
Sep 27, 2027
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 G-MOPS™ Plus
VITROLIFE Handling Pipette
VITROLIFE HYASE™ - 10X
G-RINSE ™
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-MOPS ™ PLUS
VITROLIFE SWEDEN AB
Gx-IVF ™
VITROLIFE SWEDEN AB
Gx-TL ™
VITROLIFE SWEDEN AB
VITROLIFE SpermGrad™
VITROLIFE SWEDEN AB.
VITROLIFE G-2™ Plus
VITROLIFE SWEDEN AB.

