HUBIOMED Synergy Aspirator - Indonesia BPOM Medical Device Registration
HUBIOMED Synergy Aspirator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505320189. The device is manufactured by HUBIOMED INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is AKSATA MARGA MAKMUR.
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
HUBIOMED INC.Country of Origin
Korea
Authorized Representative
AKSATA MARGA MAKMURAR Address
Foresta Business Loft 6 Unit 1, BSD City
Registration Date
Dec 20, 2024
Expiry Date
Mar 18, 2027
Product Type
Therapeutic Cardiology Equipment
Embolectomy catheter.
Non Electromedic Sterile
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