Pure Global

OF Cement - Indonesia BPOM Medical Device Registration

OF Cement is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302124434. The device is manufactured by LABORATORIOS SL S.A from Argentina, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. RONTHKARD SPINETION 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 : D
OF Cement

AF Cement

Analysis ID: AKL 31302124434

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Argentina

Authorized Representative

PT. RONTHKARD SPINETION INDONESIA

AR Address

JL. Gubeng Kertajaya X NO. 61 B

Registration Date

Jan 02, 2025

Expiry Date

Oct 20, 2029

Product Type

Prosthetic Orthopedic Equipment

Polymethylmethacrylate (PMMA) bone cement with drug

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing