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LeMaitre LifeSpan ePTFE Vascular Graft - Indonesia BPOM Medical Device Registration

LeMaitre LifeSpan ePTFE Vascular Graft is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503320358. The device is manufactured by LEMAITRE VASCULAR, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BISAWI GROWS IN HARMONY.

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BPOM Registered
Risk Class Kelas Resiko : C
LeMaitre LifeSpan ePTFE Vascular Graft
Analysis ID: AKL 20503320358

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

BISAWI GROWS IN HARMONY

AR Address

Graha Kencana Blok EU Jl. Raya Perjuangan No.88 Kebun Jeruk Jakarta Barat

Registration Date

Dec 14, 2023

Expiry Date

Dec 31, 2025

Product Type

Prosthetic Cardiology Equipment

Vascular graft prosthesis

Non Electromedic Sterile

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