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PRO-VMK III Ventilator - Indonesia BPOM Medical Device Registration

PRO-VMK III Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403027080. The device is manufactured by ACOMA MEDICAL INDUSTRY CO., LTD. OMIYA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.

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
PRO-VMK III Ventilator
Analysis ID: AKL 20403027080

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. INDOMEDIK NIAGA PERKASA

AR Address

Jl. Raya Kebayoran Lama No.35 RT.008 RW.001 Kelurahan Sukabumi Selatan, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta

Registration Date

May 16, 2023

Expiry Date

Apr 23, 2027

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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