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SAMMORA Medical Mask - Indonesia BPOM Medical Device Registration

SAMMORA Medical Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603121820. The device is manufactured by GUANDONG HAIOU MEDICAL APPARATUS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SINTHE UTAMA 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
SAMMORA Medical Mask

SAMMORA Masker Medis

Analysis ID: AKL 21603121820

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

SINTHE UTAMA INDONESIA

AR Address

Jl. Semangat No. 73 B Rt.017/ Rw.011 Kelurahan Mangga Dua Selatan Kecamatan Sawah Besar

Registration Date

Apr 05, 2021

Expiry Date

Feb 17, 2026

Product Type

Surgical Equipment

Surgical apparel.

Non Electromedic Sterile

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