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VISTAR Reusable Blood Pressure Cuff - Indonesia BPOM Medical Device Registration

VISTAR Reusable Blood Pressure Cuff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320860. The device is manufactured by SHENZHEN VISTAR MEDICAL SUPPLIES CO. LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDISTRON ENERGY.

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
VISTAR Reusable Blood Pressure Cuff
Analysis ID: AKL 20501320860

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

MEDISTRON ENERGY

AR Address

Ruko Cinere Terrace Commercial Blok JC No. 5, Jl. Telaga Warna, Kecamatan Cinere, Kelurahan Pangkalan Jati

Registration Date

Oct 07, 2024

Expiry Date

Sep 13, 2027

Product Type

Diagnostic Cardiology Equipment

Blood pressure cuff.

Non Electromedic Non Sterile

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