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UPPER Rapid Quantitative Determination for Microalbuminuria by DIGFA Method (A-SPOT) - Indonesia BPOM Medical Device Registration

UPPER Rapid Quantitative Determination for Microalbuminuria by DIGFA Method (A-SPOT) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305910317. The device is manufactured by SHANGHAI UPPER BIOTECH PHARMA CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GOLDEN MEDIKA MANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : B
UPPER Rapid Quantitative Determination for Microalbuminuria by DIGFA Method (A-SPOT)
Analysis ID: AKL 20305910317

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GOLDEN MEDIKA MANDIRI

AR Address

Jl. Raya Kalirungkut 27 Blok C-65

Registration Date

Feb 20, 2023

Expiry Date

Jan 31, 2025

Product Type

Immunological Test System

Albumin immunological test system.

Invitro Diagnostics

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DJ Fang

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