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SALTER LABS Nebulizer - Indonesia BPOM Medical Device Registration

SALTER LABS Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403811230. The device is manufactured by SALTER LABS DE MEXICO DE S.A DE C.V. from Mexico, 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
SALTER LABS Nebulizer
Analysis ID: AKL 20403811230

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

AMPM HEALTHCARE INDONESIA

AR Address

Jl.Cengkeh Kav.16 No.29-30

Registration Date

May 20, 2022

Expiry Date

Dec 06, 2026

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Electromedic Non Sterile

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