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CONMED Aer Defense Filter One - Indonesia BPOM Medical Device Registration

CONMED Aer Defense Filter One is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21604125094. The device is manufactured by CONSOLIDATED MEDICAL EQUIPMENT COMPANY from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HOSPI MEDIK 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 : B
CONMED Aer Defense Filter One
Analysis ID: AKL 21604125094

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

HOSPI MEDIK INDONESIA

AR Address

Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520

Registration Date

Dec 18, 2023

Expiry Date

Jul 22, 2027

Product Type

Therapeutic Surgical Equipment

Air-handling apparatus for a surgical operating room.

Non Radiation Electromedics

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