HEMOCHRON APTT Cuvettes - Indonesia BPOM Medical Device Registration
HEMOCHRON APTT Cuvettes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207718738. The device is manufactured by ACCRIVA DIAGNOSTICS INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DEMKA SAKTI.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
ACCRIVA DIAGNOSTICS INC.Country of Origin
United States
Authorized Representative
DEMKA SAKTIAR Address
JLN. TANAH ABANG III/19 A-B, RT.002/RW.003
Registration Date
Nov 04, 2024
Expiry Date
Dec 31, 2028
Product Type
Haematology Package and Kit
Partial thromboplastin time tests.
Invitro Diagnostics
HEMOCHRON ACT-LR Cuvettes
DIRECTCHECK Whole Blood Control
HEMOCHRON Jr. Citrate Activated Partial Thromboplastin Time (Citrate APTT) Cuvettes
DIRECTCHECK Whole Blood Control
HEMOCHRON PT Cuvettes
AVOXIMETER 1000E Whole Blood Oximeter and Accessories
HEMOCHRON ACT+ Cuvettes
HEMOCHRON Citrate PT Cuvettes
HEMOCHRON Celite ACT Tubes
MTC Heat And Moisture Exchanger
MEDIC TRADE CO.,LTD
ASETRONICS LED Surgical Light
ASETRONICS ADVANCED SWISS ELECTRONICS
ASETRONICS ASELight 120
ASETRONICS AT
ASETRONICS LED Examination Light
ASETRONICS AG.
DENYERS Operating Table
DENYERS INTERNATIONAL
DENYERS Operating Table
DENYERS INTERNATIONAL
DENYERS Slide-top Operating Table
DENYERS INTERNATIONAL
HEMOCHRON ACT-LR Cuvettes
ACCRIVA DIAGNOSTICS INC.
DIRECTCHECK Whole Blood Control
ACCRIVA DIAGNOSTICS INC.
DIRECTCHECK Whole Blood Control
ACCRIVA DIAGNOSTICS INC.

