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RESPIMER Baby Decongestant - Indonesia BPOM Medical Device Registration

RESPIMER Baby Decongestant is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704514315. The device is manufactured by LABORATORY OF THE SEA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTERBAT.

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
RESPIMER Baby Decongestant
Analysis ID: AKL 20704514315

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

France

Authorized Representative

PT. INTERBAT

AR Address

Jl. H. R. Moch. Mangundiprojo No. 1, Buduran - Sidoarjo

Registration Date

Sep 10, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Ear, Nose and Throat Equipment

Nasal irrigation solution

Non Electromedic Sterile

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