SQUID34 Liquid Embolic Agent - Indonesia BPOM Medical Device Registration
SQUID34 Liquid Embolic Agent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003420054. The device is manufactured by EMBO-FLUSSIGKEITEN A.G. from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDIKON MAIN PHARMALAB.
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
EMBO-FLUSSIGKEITEN A.G.Country of Origin
Switzerland
Authorized Representative
PT. MEDIKON MAIN PHARMALABAR Address
JLN. RAYA PASAR MINGGU NO 15, RT.001/07
Registration Date
Jun 21, 2024
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Neurology Equipment
Neurovascular embolization device.
Non Electromedic Sterile
CATCHView Thromboembolectomy System
BALT EXTRUSION SAS
MAYA NC PTCA Catheter
ARTHESYS
MAYA NC PTCA Catheter
ARTHESYS
MAYA PTCA Catheter
ARTHESYS
MAYA PTCA Catheter
ARTHESYS
ARTHESYS Y Connector PSTI
ARTHESYS
SILK VISTA Baby Intracranial Self Expandable Stent
BALT EXTRUSION SAS
LEO+ Intracranial Self Expandable Stent and Delivery System
BALT EXTRUSION SAS
MITIGATOR Sirolimus Eluting Coronary Stent System
ENVISION SCIENTIFIC PVT., LTD.
PEGASE Aspiration Catheter
ARTHESYS