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KLFMED Blood Transfusion Set - Indonesia BPOM Medical Device Registration

KLFMED Blood Transfusion Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221041. The device is manufactured by WENZHOU KLF MEDICAL PLASTICS CO., LTD.. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDICAL GREY INTERNATIONAL.

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
KLFMED Blood Transfusion Set
Analysis ID: AKL 20902221041

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDICAL GREY INTERNATIONAL

AR Address

JL. KALIMANTAN NO 22 GKB MANYAR

Registration Date

Sep 21, 2022

Expiry Date

Jun 30, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

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