CELLPACK ™ DCL - Indonesia BPOM Medical Device Registration
CELLPACK ™ DCL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208912298. The device is manufactured by SYSMEX ASIA PACIFIC PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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 ASIA PACIFIC PTE., LTD.Country of Origin
Singapore
Authorized Representative
SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Jun 06, 2024
Expiry Date
Jan 16, 2028
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
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Eightcheck-3WP-L
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CELLPACK
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STROMATOLYSER-4DL
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HISCL HBeAg Assay Kit
JAPAN LYOPHILIZATION LABORATORY.
SYSMEX CELLPACK ™ DFL
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TruLab Urine Level 2
DIASYS DIAGNOSTIC SYSTEMS GMBH
TruLab Urine Level 1
DIASYS DIAGNOSTIC SYSTEMS GMBH

