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DOSI-FUSER Portable Elastomeric Infuser - Indonesia BPOM Medical Device Registration

DOSI-FUSER Portable Elastomeric Infuser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902718088. The device is manufactured by LEVENTON, S.A.U. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AMPM HEALTHCARE 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
DOSI-FUSER Portable Elastomeric Infuser
Analysis ID: AKL 20902718088

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

LEVENTON, S.A.U.

Country of Origin

Spain

Authorized Representative

AMPM HEALTHCARE INDONESIA

AR Address

Jl.Cengkeh Kav.16 No.29-30

Registration Date

Mar 22, 2022

Expiry Date

Nov 01, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Electromedic Sterile

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