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AMBIX INTROCATH - Indonesia BPOM Medical Device Registration

AMBIX INTROCATH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902916443. The device is manufactured by PHS MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
AMBIX INTROCATH
Analysis ID: AKL 20902916443

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

PHS MEDICAL GMBH

Country of Origin

Germany

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

Oct 07, 2019

Expiry Date

Mar 08, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Percutaneous, implanted, long-term intravascular catheter.

Non Electromedic Sterile

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