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GEA Medical Air Compressor - Indonesia BPOM Medical Device Registration

GEA Medical Air Compressor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20404220005. The device is manufactured by NINGBO DAVID MEDICAL DEVICE CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.

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
GEA Medical Air Compressor
Analysis ID: AKL 20404220005

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Jan 25, 2022

Expiry Date

Jan 25, 2025

Product Type

Other Anesthesia Equipment

Portable air compressor.

Non Radiation Electromedics

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