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VOLUMAT MC AGILIA INT - Indonesia BPOM Medical Device Registration

VOLUMAT MC AGILIA INT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902112392. The device is manufactured by FRESENIUS VIAL. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
VOLUMAT MC AGILIA INT
Analysis ID: AKL 20902112392

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

FRESENIUS VIAL.

Country of Origin

France

Authorized Representative

PT. FRESENIUS KABI INDONESIA

AR Address

Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870

Registration Date

Mar 22, 2020

Expiry Date

Sep 10, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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