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GEA Lady Bug Compressor Nebulizer - Indonesia BPOM Medical Device Registration

GEA Lady Bug Compressor Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20404911055. The device is manufactured by BESMED HEALTH BUSINESS CORPORATION from Taiwan (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 Lady Bug Compressor Nebulizer
Analysis ID: AKL 20404911055

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Nov 25, 2021

Expiry Date

Nov 24, 2024

Product Type

Other Anesthesia Equipment

Portable air compressor.

Non Radiation Electromedics

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