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PHARMA-ALGI F - Indonesia BPOM Medical Device Registration

PHARMA-ALGI F is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603615500. The device is manufactured by PHARMAPLAST S.A.E. from Egypt, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GLOBAL DISPOMEDIKA.

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
PHARMA-ALGI F
Analysis ID: AKL 21603615500

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PHARMAPLAST S.A.E.

Country of Origin

Egypt

Authorized Representative

GLOBAL DISPOMEDIKA

AR Address

Jl. Penjernihan 1 No. 38 Lt. 2

Registration Date

Jul 06, 2023

Expiry Date

Jan 06, 2027

Product Type

Surgical Equipment

Occlusive wound dressing

Non Electromedic Sterile

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