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PULMODYNE HME Filters - Indonesia BPOM Medical Device Registration

PULMODYNE HME Filters is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220845. The device is manufactured by ENGINEERED MEDICAL SYSTEM MALAYSIAN SDN BHD from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAVINDRA PUTRAPRATAMA.

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 : B
PULMODYNE HME Filters
Analysis ID: AKL 20403220845

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. RAVINDRA PUTRAPRATAMA

AR Address

Pusat Niaga Duta Mas Fatmawati Blok B2-18. Jl. Fatmawati 39 - Cipete Utara Jakarta 12150

Registration Date

Nov 18, 2022

Expiry Date

Jul 29, 2024

Product Type

Therapeutic Anesthesia Equipment

Breathing circuit bacterial filter.

Non Electromedic Non Sterile

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