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SUPERA Peripheral Stent System - Indonesia BPOM Medical Device Registration

SUPERA Peripheral Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503610512. The device is manufactured by ABBOTT VASCULAR from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
SUPERA Peripheral Stent System
Analysis ID: AKL 30503610512

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

ABBOTT VASCULAR

Country of Origin

United States

Authorized Representative

PT. ABBOTT PRODUCTS INDONESIA

AR Address

WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA

Registration Date

Oct 26, 2021

Expiry Date

Sep 11, 2025

Product Type

Prosthetic Cardiology Equipment

Coronary stent

Non Electromedic Sterile

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