VITROLIFE Culture Dish - Indonesia BPOM Medical Device Registration
VITROLIFE Culture Dish is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105713137. The device is manufactured by HERTART APS. from Denmark, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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
HERTART APS.Country of Origin
Denmark
Authorized Representative
PT. DIPA PHARMALAB INTERSAINSAR Address
Jalan Raya Kebayoran Lama No. 28
Registration Date
Apr 12, 2021
Expiry Date
Nov 11, 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 Serological Pipette
VITROLIFE SWEDEN AB
VITROLIFE Micro-Droplet Culture Dish
VITROLIFE SWEDEN AB

