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AMIKA Pump Set Bag Set - Indonesia BPOM Medical Device Registration

AMIKA Pump Set Bag Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902512003. The device is manufactured by CLINICO MEDICAL SP. Z.O.O from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
AMIKA Pump Set Bag Set
Analysis ID: AKL 20902512003

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Poland

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

Aug 28, 2019

Expiry Date

May 16, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Electromedic Sterile

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