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DUODERM CGF Dressing - Indonesia BPOM Medical Device Registration

DUODERM CGF Dressing is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603024762. The device is manufactured by CONVATEC DOMINICAN REPUBLIC, INC. from Dominican, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PHARMINDO LESTARI AWARD.

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
DUODERM CGF Dressing
Analysis ID: AKL 11603024762

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Dominican

Authorized Representative

PT. PHARMINDO LESTARI AWARD

AR Address

Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara, DKI Jakarta

Registration Date

Aug 24, 2020

Expiry Date

Jun 22, 2025

Product Type

Surgical Equipment

Hydrophilic wound dressing.

Non Electromedic Sterile

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