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EAGLE PTCA Guide Wire - Indonesia BPOM Medical Device Registration

EAGLE PTCA Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505024850. The device is manufactured by UMBRA MEDICAL PRODUCTS INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : C
EAGLE PTCA Guide Wire
Analysis ID: AKL 20505024850

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Apr 09, 2021

Expiry Date

Jan 01, 2024

Product Type

Therapeutic Cardiology Equipment

Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Non Electromedic Sterile

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