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AIR LIQUIDE Suction Pump - Indonesia BPOM Medical Device Registration

AIR LIQUIDE Suction Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603211359. The device is manufactured by AIR LIQUIDE MEDICAL SYSTEMS S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ESA MEDIKA MANDIRI.

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
AIR LIQUIDE Suction Pump
Analysis ID: AKL 21603211359

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. ESA MEDIKA MANDIRI

AR Address

ESA 8 Building, 10th Floor, Jl. Ir. Soekarno Kavling 3-5

Registration Date

Sep 17, 2020

Expiry Date

Apr 30, 2024

Product Type

Surgical Equipment

Powered suction pump.

Non Radiation Electromedics

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