BIOSYNEX Ampliquick Fecal Pretreatment - Indonesia BPOM Medical Device Registration
BIOSYNEX Ampliquick Fecal Pretreatment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302320346. The device is manufactured by BIOSYNEX SA from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PACIFIC SAINTIFINDO.
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 : 1
Manufacturer
BIOSYNEX SACountry of Origin
France
Authorized Representative
PT. PACIFIC SAINTIFINDOAR Address
PASIFIK SAINTIFINDO
Registration Date
Aug 24, 2023
Expiry Date
Sep 07, 2024
Product Type
Microbiology Equipment
Transport culture medium.
Invitro Diagnostics
CapnoPen CP-001k
CAPNOPHARM GMBH
RAND CH24 ROUND SILICONE CATHETER
RAND S.P.A
RAND PERFORMER 3
RAND S.P.A
VITASSAY qPCR High-Risk HPVs
VITASSAY HEALTHCARE S.L.U
BIOSYNEX Ampliquick Helminths
BIOSYNEX SA
BIOSYNEX Ampliquick Protozoans
BIOSYNEX SA
BIOSYNEX Ampliquick STI Panel I
BIOSYNEX Ltd.
BIOSYNEX Ampliquick Sample Treatment
BIOSYNEX SA
BIOSYNEX AMPLIQUICK Sars Cov 2
BIOSYNEX Ltd.
BIOSYNEX AMPLIQUICK Lysis
BIOSYNEX Ltd.

