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FRESENIUS Agilia SP TIVA Wifi ID - Indonesia BPOM Medical Device Registration

FRESENIUS Agilia SP TIVA Wifi ID is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902812733. The device is manufactured by FRESENIUS VIAL. from France, 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
FRESENIUS Agilia SP TIVA Wifi ID
Analysis ID: AKL 20902812733

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

FRESENIUS VIAL.

Country of Origin

France

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

Sep 05, 2023

Expiry Date

Apr 21, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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