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PERIFIX Soft Tip Catheter - Indonesia BPOM Medical Device Registration

PERIFIX Soft Tip Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403512601. The device is manufactured by B.BRAUN MEDICAL INDUSTRIES SDN. BHD from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
PERIFIX Soft Tip Catheter
Analysis ID: AKL 20403512601

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Malaysia

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

Oct 31, 2023

Expiry Date

Jul 13, 2026

Product Type

Therapeutic Anesthesia Equipment

Anesthesia conduction kit.

Non Electromedic Sterile

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