Pure Global

TRAUFIX Titanium Nails - Indonesia BPOM Medical Device Registration

TRAUFIX Titanium Nails is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302520002. The device is manufactured by FIXIER, S.A. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ARJAYA LANGGENG MEDIKA.

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
TRAUFIX Titanium Nails
Analysis ID: AKL 21302520002

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

ARJAYA LANGGENG MEDIKA

AR Address

GRAHA SIMATUPANG TOWER 2C, LANTAI 4. JL. TB. SIMATUPANG KAV. 38 Kode Pos: 12540

Registration Date

Jan 03, 2025

Expiry Date

Dec 31, 2026

Product Type

Prosthetic Orthopedic Equipment

Intramedullary fixation rod.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing