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BiPAP A40 Ventilator - Indonesia BPOM Medical Device Registration

BiPAP A40 Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403413899. The device is manufactured by RESPIRONICS INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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
BiPAP A40 Ventilator
Analysis ID: AKL 20403413899

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

RESPIRONICS INC.

Country of Origin

United States

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2

Registration Date

Aug 09, 2023

Expiry Date

May 11, 2027

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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