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GENOSS DES Sirolimus Eluting Coronary Stent System - Indonesia BPOM Medical Device Registration

GENOSS DES Sirolimus Eluting Coronary Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503917418. The device is manufactured by COMRADE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ICT WORLDWIDE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
GENOSS DES Sirolimus Eluting Coronary Stent System
Analysis ID: AKL 30503917418

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

COMRADE CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. ICT WORLDWIDE INDONESIA

AR Address

Gedung Annex RS Jakarta Lt. 3, Jl. Jenderal Sudirman Kav. 49, Kel. Karet Semanggi, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos 12930

Registration Date

Jun 25, 2023

Expiry Date

May 16, 2028

Product Type

Prosthetic Cardiology Equipment

Drug eluting stent

Non Electromedic Sterile

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