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GEA Non Rebreathing Mask - Indonesia BPOM Medical Device Registration

GEA Non Rebreathing Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403321075. The device is manufactured by HANGZHOU SUPERDS INDUSTRY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. 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 : A
GEA Non Rebreathing Mask
Analysis ID: AKL 10403321075

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Jul 24, 2024

Expiry Date

Jul 22, 2027

Product Type

Therapeutic Anesthesia Equipment

Nonrebreathing mask.

Non Electromedic Non Sterile

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