PRIMELINE Diluent Reagent 3-Diff - Indonesia BPOM Medical Device Registration
PRIMELINE Diluent Reagent 3-Diff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320450. The device is manufactured by AEHEALTH LIMITED from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTI SARANA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AEHEALTH LIMITEDCountry of Origin
China
Authorized Representative
PT. MULTI SARANA MEDIKAAR Address
Komp. Gading Bukit Indah Jl. Bukit Gading Raya Blok B Kav. No.1
Registration Date
Feb 23, 2023
Expiry Date
Feb 22, 2026
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
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