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Regenerate Machine - Indonesia BPOM Medical Device Registration

Regenerate Machine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203025959. The device is manufactured by HUMAN BRAIN WAVE SRL from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. REGENESIS 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 : A
Regenerate Machine

Rigenera Machine

Analysis ID: AKL 10203025959

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Italy

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Panglima Polim Raya Blok B III/107, Jakarta Selatan

Registration Date

Oct 07, 2020

Expiry Date

Jul 08, 2025

Product Type

Pathology Equipment and Accessories

Tissue processing equipment

Invitro Diagnostics

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