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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
FIXIER, S.A. DE C.V.Country of Origin
Mexico
Authorized Representative
ARJAYA LANGGENG MEDIKAAR 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
TRAUFIX Screws for Titanium Locking Nails
FIXIER, S.A. DE C.V.
MVX Radiopaque Bone Cement
TEKNIMED S.A.S
TRAUFIX Screws for Titanium Osteosynthesis
FIXIER, S.A. DE C.V.
ReBorn Essence Venus Cervical Intervertebral Cage
BAUI BIOTECH CO., LTD.
MEDINAUT Plus Kyphoplasty System
IMEDICOM CO., LTD.
ReBorn Essence Lumbar Fixation System (2)
BAUI BIOTECH CO., LTD.
ReBorn Essence Posterior Cervical Fixation System
BAUI BIOTECH CO., LTD.
ReBorn Essence Nova Spinal Fixation System (1)
BAUI BIOTECH CO., LTD.

