Pure Global

TRABECULAR METAL ™ Acetabular Revision System (TMARS) Cage - Indonesia BPOM Medical Device Registration

TRABECULAR METAL ™ Acetabular Revision System (TMARS) Cage is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302020556. The device is manufactured by ZIMMER GMBH from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KALMED SEJAHTERA 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
TRABECULAR METAL ™ Acetabular Revision System (TMARS) Cage
Analysis ID: AKL 21302020556

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ZIMMER GMBH

Country of Origin

Switzerland

Authorized Representative

PT. KALMED SEJAHTERA INDONESIA

AR Address

JL.TAMAN MINI PINTU 2 NO. 2, RT. 006 RW. 004

Registration Date

Sep 17, 2024

Expiry Date

Dec 08, 2026

Product Type

Prosthetic Orthopedic Equipment

Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing