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GENTEC Suction Kits - Indonesia BPOM Medical Device Registration

GENTEC Suction Kits is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903221475. The device is manufactured by GENTEC (SHANGHAI) CORPORATION from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISTRON ENERGY.

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
GENTEC Suction Kits
Analysis ID: AKL 20903221475

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDISTRON ENERGY

AR Address

Ruko Cinere Terrace Commercial Blok JC No. 5, Jl. Telaga Warna

Registration Date

Dec 26, 2022

Expiry Date

Dec 31, 2025

Product Type

General Hospital Equipment and Other Individuals

Vacuum-powered body fluid suction apparatus

Non Electromedic Non Sterile

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