CUSTODIOL Perfusion Solution - Indonesia BPOM Medical Device Registration
CUSTODIOL Perfusion Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805112066. 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
Jalan Raya Kebayoran Lama No. 28
Registration Date
Aug 19, 2019
Expiry Date
May 10, 2024
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
RAPIDWARMโข Cleave
VITROLIFE SWEDEN AB.
G-MOPSโข
VITROLIFE SWEDEN AB.
EMBRYOGLUE
VITROLIFE SWEDEN AB.
VITROLIFE G-MOPSโข Plus
VITROLIFE SWEDEN AB.
VITROLIFE Centrifuge Tube
VITROLIFE SWEDEN AB
VITROLIFE Pasteur Pipette
VITROLIFE SWEDEN AB
VITROLIFE 5 WELL Culture Dish
VITROLIFE SWEDEN AB
VITROLIFE Serological Pipette
VITROLIFE SWEDEN AB

