Gx-TL ™ - Indonesia BPOM Medical Device Registration
Gx-TL ™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105320116. 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 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 18, 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 5 WELL Culture Dish
VITROLIFE Micro-Droplet Culture Dish
SAMPLE TUBE
VITROLIFE Collection Dish
ICSI Dish
VITROLIFE Serological Pipette
VITROLIFE Centre Well Dish
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
VITROLIFE SpermGrad™
VITROLIFE SWEDEN AB.
SPERMRINSE ™
VITROLIFE SWEDEN AB.
VITROLIFE G-2™ Plus
VITROLIFE SWEDEN AB.

