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PENUMBRA PUMP MAX - Indonesia BPOM Medical Device Registration

PENUMBRA PUMP MAX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003719354. The device is manufactured by PENUMBRA INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BISAWI GROWS IN HARMONY.

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BPOM Registered
Risk Class Kelas Resiko : C
PENUMBRA PUMP MAX
Analysis ID: AKL 21003719354

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

PENUMBRA INC.

Country of Origin

United States

Authorized Representative

PT. BISAWI GROWS IN HARMONY

AR Address

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

Registration Date

Dec 05, 2023

Expiry Date

Dec 31, 2026

Product Type

Therapeutic Neurology Equipment

Neurovascular embolization device.

Non Radiation Electromedics

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