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MEIJI Medical Negative Pressure Suction Device - Indonesia BPOM Medical Device Registration

MEIJI Medical Negative Pressure Suction Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903321900. The device is manufactured by GUANGDONG MEIJI BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EUPHRATES WITH.

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
MEIJI Medical Negative Pressure Suction Device
Analysis ID: AKL 20903321900

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. EUPHRATES WITH

AR Address

Ruko Gardenia kav 1, jln. parigi raya no 75 sukabakti curug 15810

Registration Date

May 05, 2023

Expiry Date

May 25, 2026

Product Type

General Hospital Equipment and Other Individuals

Vacuum-powered body fluid suction apparatus.

Non Radiation Electromedics

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