FIGULLA® Flex II PFO Occluder - Indonesia BPOM Medical Device Registration
FIGULLA® Flex II PFO Occluder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503819498. The device is manufactured by OCCLUTECH GMBH. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.
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
OCCLUTECH GMBH.Country of Origin
Germany
Authorized Representative
PT. MULTIDAYA MEDIKAAR Address
RUKAN NIAGA GUNUNG SAHARI BLOK B-1
Registration Date
Feb 22, 2023
Expiry Date
Dec 13, 2027
Product Type
Prosthetic Cardiology Equipment
Cardiac occluder
Non Electromedic Sterile
ZERO-GRAVITY Radiation Protection System
TIDI PRODUCTS, LLC.
PROLONG Guiding Extension Catheter
SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD.
BRAILE Hemoconcentrator
BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA
FIGULLA Flex II ASD Occluder Procedure Pack
OCCLUTECH INTERNATIONAL AB
INT Introducer Set
SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD.
BRAILE Blood Reservoir
BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA
MEMBRANE OXYGENATOR OXYPRIME DUO
BRAILE BIOMÉDICA INDÍSTRIA COMéRCIO E REPRESENTAÇÕES LTDA.
BRAILE BIOMEDICA Arterial Blood Filter
BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA
BRAILE BIOMEDICA Membrane Oxygenator
BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA
OCCLUTECH Sizing Balloon
OCCLUTECH GMBH.