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GOODTEC Angiographic Diagnostic Catheter - Indonesia BPOM Medical Device Registration

GOODTEC Angiographic Diagnostic Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501520038. The device is manufactured by GOODMAN CO., LTD. GOODMAN SEKI FACILITY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAKO TWO MEDICAL.

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BPOM Registered
Risk Class Kelas Resiko : C
GOODTEC Angiographic Diagnostic Catheter
Analysis ID: AKL 20501520038

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. MAKO TWO MEDICAL

AR Address

Rukan Avenue 8 No. 125 dan 127 lantai 1, Jakarta Garden City, Kel. Cakung Timur, Kec. Cakung, Kota Jakarta Timur, Provinsi DKI Jakarta, Kode Pos: 13910

Registration Date

Jan 23, 2025

Expiry Date

Sep 30, 2029

Product Type

Diagnostic Cardiology Equipment

Diagnostic intravascular catheter.

Non Electromedic Sterile

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