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Accupoint Blood Transfusion Bag Single - Indonesia BPOM Medical Device Registration

Accupoint Blood Transfusion Bag Single is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420167. The device is manufactured by SUZHOU LAISHI TRANSFUSION EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIGMA PRIMARY CORE.

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
Accupoint Blood Transfusion Bag Single
Analysis ID: AKL 20209420167

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SIGMA PRIMARY CORE

AR Address

JL. IR. H. JUANDA RT. 002, RW. 008

Registration Date

May 07, 2024

Expiry Date

Dec 04, 2028

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Empty container for the collection and processing of blood and blood components.

Non Electromedic Sterile

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DJ Fang

DJ Fang

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