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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.

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BPOM Registered
Risk Class Kelas Resiko : C
HUBIOMED Synergy Aspirator
Analysis ID: AKL 20505320189

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

HUBIOMED INC.

Country of Origin

Korea

Authorized Representative

AKSATA MARGA MAKMUR

AR 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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