CUSTODIOL -CE - Indonesia BPOM Medical Device Registration
CUSTODIOL -CE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420139. The device is manufactured by DR. FRANZ KOHLER CHEMIE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIPA PHARMALAB INTERSAINS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DR. FRANZ KOHLER CHEMIE GMBHCountry of Origin
Germany
Authorized Representative
PT. DIPA PHARMALAB INTERSAINSAR Address
Jl. Raya Kebayoran Lama No. 28, Kebayoran Lama,Jakarta Selatan, DKl Jakarta, kode pos : 12210
Registration Date
Mar 13, 2024
Expiry Date
Oct 30, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Isolated kidney perfusion and transport system and accessories.
Non Electromedic Sterile
VITROLIFE G-1 Plus
VITROLIFE SWEDEN AB.
IALURIL Prefill
IBSA FARMACEUTICI ITALIA, SRL
RAPIDWARM™ Cleave
VITROLIFE SWEDEN AB.
G-MOPS™
VITROLIFE SWEDEN AB.
VITROLIFE G-MOPS™ Plus
VITROLIFE SWEDEN AB.
EMBRYOGLUE
VITROLIFE SWEDEN AB.
VITROLIFE Centrifuge Tube
VITROLIFE SWEDEN AB
VITROLIFE Pasteur Pipette
VITROLIFE SWEDEN AB
VITROLIFE Serological Pipette
VITROLIFE SWEDEN AB
VITROLIFE Micro-Droplet Culture Dish
VITROLIFE SWEDEN AB