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ProShield N-95 Medium - Indonesia BPOM Medical Device Registration

ProShield N-95 Medium is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903124868. The device is manufactured by SAN-M PACKAGE CO. LTD from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ESSITY HYGIENE AND HEALTH INDONESIA.

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
ProShield N-95 Medium
Analysis ID: AKL 20903124868

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

AR Address

Green Office Park 6, Wing B, lantai 1, Zona 8-12, BSD Green Office Park, BSD City, Desa Sampora, Kec. Cisauk, Kab.Tangerang 15345

Registration Date

Aug 09, 2021

Expiry Date

Jun 23, 2026

Product Type

General Hospital Equipment and Other Individuals

Filtering facepiece respirator for use by the general public in public health medical emergencies.

Non Electromedic Non Sterile

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