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MG Disposable Hemoperfusion Cartridge - Indonesia BPOM Medical Device Registration

MG Disposable Hemoperfusion Cartridge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805412545. The device is manufactured by FOSHAN BIOSUN MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ORIONTAMA JAYA.

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 : C
MG Disposable Hemoperfusion Cartridge
Analysis ID: AKL 20805412545

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ORIONTAMA JAYA

AR Address

Jl. Sutomo No. 122-124, Medan

Registration Date

Feb 27, 2023

Expiry Date

Feb 02, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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