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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.

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BPOM Registered
Risk Class Kelas Resiko : B
PRIMELINE Uric Acid, Uricase
Analysis ID: AKL 20101221085

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

MULTI SARANA MEDIKA

AR 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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