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IODOSORB Powder - Indonesia BPOM Medical Device Registration

IODOSORB Powder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603714443. The device is manufactured by PERSTORP SPECIALITY CHEMICALS AB. from Sweden, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ENSEVAL PUTERA MEGATRADING TBK.

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 : A
IODOSORB Powder
Analysis ID: AKL 11603714443

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Sweden

Authorized Representative

ENSEVAL PUTERA MEGATRADING TBK

AR Address

Jalan Pulo Lentut No.10 Kawasan Industri Pulogadung, Jakarta Timur

Registration Date

Sep 08, 2023

Expiry Date

Dec 31, 2025

Product Type

Surgical Equipment

Hydrophilic wound dressing.

Non Electromedic Sterile

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