Pure Global

SIGNIA Forklift - Indonesia BPOM Medical Device Registration

SIGNIA Forklift is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603716547. The device is manufactured by COVIDIEN from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC 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
SIGNIA Forklift

SIGNIA Stapler

Analysis ID: AKL 21603716547

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

COVIDIEN

Country of Origin

United States

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Feb 18, 2021

Expiry Date

Jan 13, 2026

Product Type

Surgical Equipment

Implantable staple.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing