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BISOND Handheld Oximeter - Indonesia BPOM Medical Device Registration

BISOND Handheld Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502520039. The device is manufactured by SHENZHEN LE MEDICAL TECHNOLOGY , CO, LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NUSANTARA MEDIKA SUCCEEDED.

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
BISOND Handheld Oximeter
Analysis ID: AKL 20502520039

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. NUSANTARA MEDIKA SUCCEEDED

AR Address

Ruko Terrace 9 Blok A No. 29, Suvarna Sutera, Jl. Jati Utama, Kode Pos 15561

Registration Date

Jan 14, 2025

Expiry Date

Mar 26, 2027

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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