PRIMELINE Uric Acid, Uricase - Indonesia BPOM Medical Device Registration
PRIMELINE Uric Acid, Uricase is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221085. The device is manufactured by BEIJING STRONG BIOTECHNOLOGIES, INC from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTI SARANA MEDIKA.
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
BEIJING STRONG BIOTECHNOLOGIES, INCCountry of Origin
China
Authorized Representative
MULTI SARANA MEDIKAAR Address
Komp. Gading Bukit Indah Jl. Bukit Gading Raya Blok B Kav. No.1
Registration Date
Jul 25, 2022
Expiry Date
May 17, 2026
Product Type
Clinical Chemistry Test System
Uric acid test system (kit & cair)
Invitro Diagnostics
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PRIMELINE HDL Cholesterol Direct, Select inhibition
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