Pure Global

ORTHOSPEC Extracorporeal Shock Wave Therapy - Indonesia BPOM Medical Device Registration

ORTHOSPEC Extracorporeal Shock Wave Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403010009. The device is manufactured by MEDISPEC LTD. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. GRATIA JAYA MULYA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : D
ORTHOSPEC Extracorporeal Shock Wave Therapy
Analysis ID: AKL 21403010009

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MEDISPEC LTD.

Country of Origin

United States

Authorized Representative

PT. GRATIA JAYA MULYA

AR Address

Gading Park View Blok ZC.I No. 10-11 Jl. Boulevard Timur Raya

Registration Date

May 30, 2022

Expiry Date

Feb 14, 2025

Product Type

Therapeutic Physical Health Equipment

Extracorporeal shock wave treatment device

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing