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DIO IMPLANT Surgical Tool - Indonesia BPOM Medical Device Registration

DIO IMPLANT Surgical Tool is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603022578. The device is manufactured by DIO CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BINTANG SAUDARA SEMESTA JAYA.

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
DIO IMPLANT Surgical Tool
Analysis ID: AKL 10603022578

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

DIO CORPORATION

Country of Origin

Korea

Authorized Representative

PT. BINTANG SAUDARA SEMESTA JAYA

AR Address

Jl.Asia No.212 A-B, Medan

Registration Date

Aug 24, 2020

Expiry Date

Jul 30, 2024

Product Type

Surgical Dental Equipment

Dental hand instrument

Non Electromedic Non Sterile

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