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BOSTON ROTABLATOR™ Rotational Angioplasty System - Indonesia BPOM Medical Device Registration

BOSTON ROTABLATOR™ Rotational Angioplasty System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504318168. The device is manufactured by BOSTON SCIENTIFIC CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BOSTON SCIENTIFIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
BOSTON ROTABLATOR™ Rotational Angioplasty System
Analysis ID: AKL 20504318168

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BOSTON SCIENTIFIC INDONESIA

AR Address

Gd Tamara Center Lantai 8 Suite 805 Jl. Jenderal Sudirman Kav. 24 Kel. Karet Kec. Setiabudi Telp. 021-5272990, Fax. 021-5272991

Registration Date

Jan 31, 2018

Expiry Date

Dec 31, 2023

Product Type

Surgical Cardiology Equipment

Intraluminal artery stripper.

Non Radiation Electromedics

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