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PURITAN BENNETT 980 Ventilator - Indonesia BPOM Medical Device Registration

PURITAN BENNETT 980 Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403713673. The device is manufactured by COVIDIEN from Ireland, 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.

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BPOM Registered
Risk Class Kelas Resiko : C
PURITAN BENNETT 980 Ventilator
Analysis ID: AKL 20403713673

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

COVIDIEN

Country of Origin

Ireland

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Aug 04, 2024

Expiry Date

Feb 20, 2029

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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