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ATRASORB Pharma - Indonesia BPOM Medical Device Registration

ATRASORB Pharma is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403124581. The device is manufactured by ATRASORB INDUSTRIA DE PRODUTOS HOSPITALARES LTDA. from Brazil, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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
ATRASORB Pharma
Analysis ID: AKL 20403124581

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Oct 17, 2024

Expiry Date

Jun 15, 2026

Product Type

Therapeutic Anesthesia Equipment

Carbon dioxide absorbent.

Non Electromedic Non Sterile

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