SM UA Reagent Kit - Indonesia BPOM Medical Device Registration

SM UA Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421374. The device is manufactured by URIT MEDICAL ELECTRONIC CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.

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BPOM Registered

Risk Class Kelas Resiko : B

SM UA Reagent Kit

Analysis ID: AKL 20101421374

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

URIT MEDICAL ELECTRONIC CO., LTD

Country of Origin

China

Authorized Representative

PT. FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No. 39, Jl. Yos Sudarso Kav. 89 Kel. Sunter Jaya, Kec. Tanjung Priok, Jakarta Utara

Registration Date

Aug 31, 2024

Expiry Date

Jul 22, 2027

Product Type

Clinical Chemistry Test System

Uric acid test system (kit & cair)

Invitro Diagnostics

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SM UA Reagent Kit - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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