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LINEAR Intra Aortic Balloon Catheter - Indonesia BPOM Medical Device Registration

LINEAR Intra Aortic Balloon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503719283. The device is manufactured by DATASCOPE, CORP. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. INDOSOPHA SAKTI.

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BPOM Registered
Risk Class Kelas Resiko : D
LINEAR Intra Aortic Balloon Catheter
Analysis ID: AKL 30503719283

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

DATASCOPE, CORP.

Country of Origin

United States

Authorized Representative

PT. INDOSOPHA SAKTI

AR Address

JL. MAMPANG PRAPATAN RAYA NO.1

Registration Date

Feb 11, 2025

Expiry Date

Dec 31, 2025

Product Type

Prosthetic Cardiology Equipment

Intra-aortic balloon and control system

Non Electromedic Sterile

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