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SZOSEN Infusion Pump - Indonesia BPOM Medical Device Registration

SZOSEN Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902814913. The device is manufactured by SHENZHEN OSEN TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRINITY ALPHA OMEGA.

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
SZOSEN Infusion Pump
Analysis ID: AKL 20902814913

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

TRINITY ALPHA OMEGA

AR Address

JL. Tanjung Duren Timur V No. 49 Jakarta Barat 11470

Registration Date

Feb 15, 2023

Expiry Date

Jan 25, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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