TECHNOWOOD SSS Guidewire - Indonesia BPOM Medical Device Registration
TECHNOWOOD SSS Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501516164. The device is manufactured by TECHNOWOOD CORPORATION KOHOKU FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BISAWI GROWS IN HARMONY.
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 : 2
Manufacturer
TECHNOWOOD CORPORATION KOHOKU FACTORYCountry of Origin
Japan
Authorized Representative
PT. BISAWI GROWS IN HARMONYAR Address
Graha Kencana Blok EU Jl. Raya Perjuangan No.88 Kebun Jeruk Jakarta Barat
Registration Date
May 06, 2021
Expiry Date
Jan 22, 2026
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
IHTEVOLVE PTCA Dilatation Catheter
IBERHOSPITEX, S.A.
VEINVU 200
MAJUTECH, INC.
INDIGO Aspiration System
PENUMBRA INC.
BENCHMARK Intracranial Access System
PENUMBRA INC.
POLYMED Huber Infusion Set
POLY MEDICURE LIMITED
MILLAU NC PTA Ballon Dilatation Catheter
CNOVATE MEDICAL B.V.
OBTURA Vascural Closure Device
MERIL LIFE SCIENCES PVT. LTD.
TRILLY PED AF Full Coated STE
EUROSETS SRL
ECMOLIFE Centrifugal Pump
EUROSETS SRL
LSI COR-KNOT MINI Device Kit
LSI SOLUTIONS INC.