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CAMI Suction Unit - Indonesia BPOM Medical Device Registration

CAMI Suction Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603221769. The device is manufactured by CAMI, Ltd. 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
CAMI Suction Unit
Analysis ID: AKL 21603221769

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CAMI, Ltd.

Country of Origin

Italy

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

Ruko Golden Boulevard Blok i No 7 BSD City

Registration Date

Aug 25, 2022

Expiry Date

Apr 01, 2027

Product Type

Surgical Equipment

Powered suction pump.

Non Radiation Electromedics

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