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B. BRAUN Meliseptol Foam Pure - Indonesia BPOM Medical Device Registration

B. BRAUN Meliseptol Foam Pure is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903111743. The device is manufactured by B. BRAUN MEDICAL AG. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
B. BRAUN Meliseptol Foam Pure
Analysis ID: AKL 20903111743

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

PT. B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Jan 29, 2020

Expiry Date

Oct 09, 2024

Product Type

General Hospital Equipment and Other Individuals

Liquid chemical sterilants/high level disinfectants.

Non Electromedic Sterile

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