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TELEFLEX PILLING CABG (Coronary) Instrument Set Standard - Indonesia BPOM Medical Device Registration

TELEFLEX PILLING CABG (Coronary) Instrument Set Standard is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10504910375. The device is manufactured by TELEFLEX MEDICAL from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SURGIKA ALKESINDO.

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BPOM Registered
Risk Class Kelas Resiko : A
TELEFLEX PILLING CABG (Coronary) Instrument Set Standard
Analysis ID: AKL 10504910375

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

TELEFLEX MEDICAL

Country of Origin

United States

Authorized Representative

SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Dec 28, 2023

Expiry Date

Dec 31, 2025

Product Type

Surgical Cardiology Equipment

Cardiovascular surgical instruments.

Non Electromedic Non Sterile

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