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SAMMORA Pulse Oximeter - Indonesia BPOM Medical Device Registration

SAMMORA Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502024292. The device is manufactured by HUNAN ACCURATE BIO-MEDICAL TECHNOLOGY 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 Pulse Oximeter
Analysis ID: AKL 20502024292

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

Aug 14, 2023

Expiry Date

Oct 22, 2027

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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