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PD PRODEVICE - Indonesia BPOM Medical Device Registration

PD PRODEVICE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402320686. The device is manufactured by HUBEI JOY BONE MEDICAL PRODUCTS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BETWEEN PARTNERS OF SELF-SUFFICIENCY.

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
PD PRODEVICE

PD PRODEVICE Gyps

Analysis ID: AKL 11402320686

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

AR Address

Jl. Pos Pengumben Raya No.8 RT.005 RW.005, Sukabumi Selatan, Kebon Jeruk, Jakarta Barat 11560

Registration Date

Apr 23, 2024

Expiry Date

Jul 05, 2026

Product Type

Prosthetic Physical Health Equipment

Prosthetic and orthotic accessory.

Non Electromedic Non Sterile

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