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PAP Ventilator - Indonesia BPOM Medical Device Registration

PAP Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220202. The device is manufactured by SHENZEN COMEN MEDICAL INSTRUMENT CO. LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FLUORESCENT ANDHIKA PARAMARTHA.

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
PAP Ventilator
Analysis ID: AKL 20403220202

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FLUORESCENT ANDHIKA PARAMARTHA

AR Address

RUKAN GADING BUKIT INDAH BLOK U / 09 RT 008 RW 015 - KOMPLEK GADING BUKIT INDAH - JL. BUKIT INDAH RAYA KELAPA GADING JAKARTA UTARA

Registration Date

Aug 07, 2024

Expiry Date

Aug 05, 2027

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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