Bi-Flex ELON POB-MA - Indonesia BPOM Medical Device Registration
Bi-Flex ELON POB-MA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320155. The device is manufactured by MEDICONTUR MEDICAL ENGINEERING LTD. from Hungary, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is SURGIKA ALKESINDO.
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 : 3
Manufacturer
MEDICONTUR MEDICAL ENGINEERING LTD.Country of Origin
Hungary
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Sep 16, 2023
Expiry Date
Dec 31, 2025
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
BI-FLEX Aspheric Hydrophilic Acrylic IOL
MEDICONTUR BI-FLEX HB Aspheric Hydrophobic Acrylic IOL
MEDICONTUR Aspheric Hydrophobic Acrylic IOL
MEDICONTUR Bi-FLEX POB-MA Aspheric Hydrophobic Acrylic IOL
MEDICONTUR TRIFOCAL Bi-Flex Liberty
SCHARIOTH MACULAR Lens
MEDICONTUR Classic Aspheric Hydrophilic Acrylic IOL
BI-FLEX ELON Toric POB-MA Hydrophobic Preloaded IOL
IDRA – Dedicated Dry Eye Platform
SBM SISTEMI S. R. L
SBM DSLC 200
SBM SISTEMI S.R.L.
SBM DEM 100
SBM SISTEMI S.R.L.
LUMENIS Digital OptiLight System
LUMENIS BE INC.
PLASMAGE
BRERA MEDICAL TECHNOLOGIES S.R.L
LITHOTRIPTER 3000 Plus
RICHARD WOLF GMBH
UFSK Surgeon's Chair surgiForce Light, with Formed Seat
UFSK-INTERNATIONAL OSYS GMBH
LUMENIS Pulse 120H, Moses 2.0
LUMENIS LTD.
MEDTRON ACCUTRON MR
MEDTRON AG.
VERSIUS Surgical System with vLimelite
CMR SURGICAL LIMITED