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MEDTRONIC ENT Burs - Indonesia BPOM Medical Device Registration

MEDTRONIC ENT Burs is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703320190. The device is manufactured by COVIDIEN from Dominican, and is classified as Risk Class Kelas Resiko : A. 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.

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BPOM Registered
Risk Class Kelas Resiko : A
MEDTRONIC ENT Burs
Analysis ID: AKL 10703320190

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

COVIDIEN

Country of Origin

Dominican

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

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

Registration Date

Feb 02, 2023

Expiry Date

Feb 16, 2027

Product Type

Ear, Nose and Throat Surgical Equipment

Ear, nose, and throat bur.

Non Electromedic Sterile

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