ICSI Pipette Micromanipulation Pipettes - Indonesia BPOM Medical Device Registration
ICSI Pipette Micromanipulation Pipettes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105818554. The device is manufactured by VITROLIFE INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DIPA PHARMALAB INTERSAINS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VITROLIFE INC.Country of Origin
United States
Authorized Representative
DIPA PHARMALAB INTERSAINSAR Address
Jalan Raya Kebayoran Lama No. 28
Registration Date
Jan 20, 2021
Expiry Date
Nov 13, 2025
Product Type
Reproductive Aids
Assisted reproduction micropipette fabrication instruments.
Invitro Diagnostics
VITROLIFE HSA-Solutionโข
VITROLIFE SWEDEN AB.
ICSIโข
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 โข PLUS
VITROLIFE SWEDEN AB
Gx-IVF โข
VITROLIFE SWEDEN AB
Gx-TL โข
VITROLIFE SWEDEN AB
RAPIDVITโข Cleave
VITROLIFE SWEDEN AB.
SPERMRINSE โข
VITROLIFE SWEDEN AB.

