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ANGIOJET Ultra Console - Indonesia BPOM Medical Device Registration

ANGIOJET Ultra Console is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505810046. The device is manufactured by BOSTON SCIENTIFIC CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BOSTON SCIENTIFIC INDONESIA.

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
ANGIOJET Ultra Console
Analysis ID: AKL 20505810046

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BOSTON SCIENTIFIC INDONESIA

AR Address

Prudential Tower lantai 28 Jl. Jend. Sudirman Kav. 79

Registration Date

Nov 25, 2022

Expiry Date

Apr 20, 2027

Product Type

Therapeutic Cardiology Equipment

Embolectomy catheter.

Non Radiation Electromedics

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