VITROLIFE Serological Pipette - Indonesia BPOM Medical Device Registration
VITROLIFE Serological Pipette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105024255. The device is manufactured by HERTART APS. from Sweden, 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
HERTART APS.Country of Origin
Sweden
Authorized Representative
PT. DIPA PHARMALAB INTERSAINSAR Address
Jalan Raya Kebayoran Lama No. 28
Registration Date
Aug 01, 2020
Expiry Date
May 18, 2025
Product Type
Reproductive Aids
Assisted reproduction labware.
Invitro Diagnostics
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 Micro-Droplet Culture Dish
VITROLIFE SWEDEN AB

