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INTRAPUR Inline Infusion Kit - Indonesia BPOM Medical Device Registration

INTRAPUR Inline Infusion Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902700099. The device is manufactured by B. BRAUN MEDICAL KFT PRODUCTION DIVISION from Hungary, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
INTRAPUR Inline Infusion Kit
Analysis ID: AKL 20902700099

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Hungary

Authorized Representative

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

Aug 07, 2024

Expiry Date

Mar 31, 2029

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set.

Non Electromedic Sterile

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