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REJIVA Biofeedback Device - Indonesia BPOM Medical Device Registration

REJIVA Biofeedback Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003128156. The device is manufactured by RIJUVEN CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. QTASNIM DIGITAL TECHNOLOGY.

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
REJIVA Biofeedback Device
Analysis ID: AKL 21003128156

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. QTASNIM DIGITAL TECHNOLOGY

AR Address

JL. PASIRLAYUNG UTARA IV NOMOR 15

Registration Date

Dec 23, 2021

Expiry Date

Jul 26, 2025

Product Type

Therapeutic Neurology Equipment

Biofeedback device.

Non Radiation Electromedics

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