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OMNIPORE Surgical Implants - Indonesia BPOM Medical Device Registration

OMNIPORE Surgical Implants is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602024966. The device is manufactured by MATRIX SURGICAL USA from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ORIONTAMA JAYA.

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.

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BPOM Registered
Risk Class Kelas Resiko : C
OMNIPORE Surgical Implants
Analysis ID: AKL 21602024966

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. ORIONTAMA JAYA

AR Address

Jl. Sutomo No. 122

Registration Date

Sep 02, 2020

Expiry Date

Feb 21, 2025

Product Type

Prosthetic Surgical Equipment

Polytetrafluoroethylene with carbon fibers composite implant material.

Non Electromedic Sterile

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