Pure Global

FULE Posterior Cervical Screw-Plate System - Indonesia BPOM Medical Device Registration

FULE Posterior Cervical Screw-Plate System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302123418. The device is manufactured by BEIJING FULE SCIENCE AND TECHNOLOGY DEVELOPMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is WIJAYA MITRA HUSADA.

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 : C
FULE Posterior Cervical Screw-Plate System
Analysis ID: AKL 21302123418

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

WIJAYA MITRA HUSADA

AR Address

Jln. Sirojul Munir, Kp Cakung, Perum Pualam Green Village, Kav 2, RT 004/03, Jatisari, Jati Asih, Kota Bekasi

Registration Date

Jun 10, 2021

Expiry Date

Aug 20, 2025

Product Type

Prosthetic Orthopedic Equipment

Spinal interlaminal fixation orthosis.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from BEIJING FULE SCIENCE AND TECHNOLOGY DEVELOPMENT CO., LTD
Products from the same manufacturer (1 products)