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B. BRAUN PRONTODERM® Foam - Indonesia BPOM Medical Device Registration

B. BRAUN PRONTODERM® Foam is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903713952. 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 PRONTODERM® Foam
Analysis ID: AKL 20903713952

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

May 04, 2021

Expiry Date

Jan 28, 2026

Product Type

General Hospital Equipment and Other Individuals

Liquid chemical sterilants/high level disinfectants.

Non Electromedic Non Sterile

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