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BARD® Polyester Felt - Indonesia BPOM Medical Device Registration

BARD® Polyester Felt is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503712510. The device is manufactured by BARD SHANNON LIMITED from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PERMATA BUNDA ARTANO.

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BPOM Registered
Risk Class Kelas Resiko : C
BARD® Polyester Felt
Analysis ID: AKL 20503712510

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PERMATA BUNDA ARTANO

AR Address

Jl. Hos. Cokroaminoto, Komp. Perkantoran CBD Ciledug Blok A3 No. 17, Ciledug 15157

Registration Date

Oct 22, 2020

Expiry Date

Dec 31, 2023

Product Type

Prosthetic Cardiology Equipment

Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene.

Non Electromedic Sterile

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