PRIMELINE Probe Cleanser 3-Diff - Indonesia BPOM Medical Device Registration
PRIMELINE Probe Cleanser 3-Diff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204320406. The device is manufactured by AEHEALTH LIMITED from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULTI SARANA MEDIKA.
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Risk Classification
Product Class
Kelas : 1
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 27, 2023
Expiry Date
Dec 31, 2026
Product Type
Reagents and Specimen Providers
General purpose reagent.
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