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BEURER Nebuliser - Indonesia BPOM Medical Device Registration

BEURER Nebuliser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403312711. The device is manufactured by BEURER GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SERENITY 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
BEURER Nebuliser
Analysis ID: AKL 20403312711

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BEURER GMBH.

Country of Origin

Germany

Authorized Representative

PT. SERENITY INDONESIA

AR Address

Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter

Registration Date

Mar 01, 2021

Expiry Date

Sep 18, 2025

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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