Pure Global

FIXIT Threaded Anchor System - Indonesia BPOM Medical Device Registration

FIXIT Threaded Anchor System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302912539. The device is manufactured by S.B.M. SAS from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ENDO INDONESIA.

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
FIXIT Threaded Anchor System
Analysis ID: AKL 21302912539

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

S.B.M. SAS

Country of Origin

France

Authorized Representative

ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Feb 07, 2023

Expiry Date

Jun 20, 2027

Product Type

Prosthetic Orthopedic Equipment

Single/multiple component metallic bone fixation appliances and accessories.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing