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CA-MI Sterilisator (Germicidal Lamp) - Indonesia BPOM Medical Device Registration

CA-MI Sterilisator (Germicidal Lamp) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903802940. The device is manufactured by CA-MI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FA ANTARES MEDIKA.

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
CA-MI Sterilisator (Germicidal Lamp)
Analysis ID: AKL 20903802940

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CA-MI S.R.L.

Country of Origin

Italy

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

Ruko Golden Boulevard Blok i No 7 BSD City

Registration Date

May 27, 2022

Expiry Date

Apr 01, 2027

Product Type

General Hospital Equipment and Other Individuals

Medical ultraviolet air purifier.

Non Radiation Electromedics

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