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BONBONE CINDERELLA - Indonesia BPOM Medical Device Registration

BONBONE CINDERELLA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402121096. The device is manufactured by DAIYA INDUSTRY CO., LTD from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SEKARGUNA MEDIKA.

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
BONBONE CINDERELLA
Analysis ID: AKL 11402121096

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Mar 01, 2021

Expiry Date

May 13, 2025

Product Type

Prosthetic Physical Health Equipment

Limb orthosis.

Non Electromedic Non Sterile

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