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WALKMAN Cannulated Screw System - Indonesia BPOM Medical Device Registration

WALKMAN Cannulated Screw System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320717. The device is manufactured by TIANJIN WALKMAN BIOMATERIAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.

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 : C
WALKMAN Cannulated Screw System
Analysis ID: AKL 21302320717

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. CEKINDO BUSINESS INTERNATIONAL

AR Address

CEKINDO BUSINESS INTERNATIONAL

Registration Date

Jun 13, 2023

Expiry Date

Nov 15, 2025

Product Type

Prosthetic Orthopedic Equipment

Smooth or threaded metallic bone fixation fastener.

Non Electromedic Non Sterile

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