SYSMEX CELLPACK DFL - Indonesia BPOM Medical Device Registration
SYSMEX CELLPACK DFL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208914152. The device is manufactured by SYSMEX CORPORATION ONO FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SYSMEX INDONESIA.
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
SYSMEX CORPORATION ONO FACTORYCountry of Origin
Japan
Authorized Representative
PT. SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Mar 27, 2023
Expiry Date
Jan 16, 2028
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
HISCL Probe Washing Solution
HISCL Washing Solution
HISCL Line Washing Solution
Concentrated Phosphate Buffer for SP pH 7.2
SYSMEX Concentrated Phosphate Buffer for SP pH 6.8
SYSMEX UF-Fluorocell CR
SYSMEX Wash Solution C-1
SYSMEX Automated Blood Coagulation Analyzer CN-6000
SYSMEX CORPORATION
XN CAL PF
DASH, INC.
SULFOLYSER
SYSMEX CORPORATION, ONO FACTORY.
POCH-PACK L PPL-200A
SYSMEX CORPORATION, ONO FACTORY.
EIGHTCHECK-3WP-H
DASH, INC.
XN-CHECK L2
DASH, INC.
SYSMEX CELLSHEATH
SYSMEX CORPORATION, ONO FACTORY.
XN-CHECKโข L3
DASH, INC.
SYSMEX CD4% easy count kit
EXBIO PRAHA, A.S.
SYSMEX Ca Cal S
SYSMEX CORPORATION, SEISHIN FACTORY.

