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GIGASEPT PAA - Indonesia BPOM Medical Device Registration

GIGASEPT PAA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903710333. The device is manufactured by BIOXAL Ltd. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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
GIGASEPT PAA
Analysis ID: AKL 20903710333

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BIOXAL Ltd.

Country of Origin

France

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Oct 05, 2023

Expiry Date

Jul 11, 2028

Product Type

General Hospital Equipment and Other Individuals

Liquid chemical sterilants/high level disinfectants.

Non Electromedic Non Sterile

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