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IMPROSAFE Blood Collection Sets - Indonesia BPOM Medical Device Registration

IMPROSAFE Blood Collection Sets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902023989. The device is manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MACROCITRA ARDANASEJATI.

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
IMPROSAFE Blood Collection Sets
Analysis ID: AKL 20902023989

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MACROCITRA ARDANASEJATI

AR Address

Rukan Taman Meruya Blok M-65 Meruya Ilir - Jakarta Barat Telp. 021-5874575, Fax. 021-5874573

Registration Date

Dec 14, 2023

Expiry Date

Jul 02, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

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