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GENTIAN Cystatin C Reagent Kit - Indonesia BPOM Medical Device Registration

GENTIAN Cystatin C Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221463. The device is manufactured by GENTIAN AS from Norway, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DHH TRADING INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
GENTIAN Cystatin C Reagent Kit
Analysis ID: AKL 20101221463

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GENTIAN AS

Country of Origin

Norway

Authorized Representative

PT. DHH TRADING INDONESIA

AR Address

Gedung World Trade Center 3, Lt. 20, Jl. Jend. Sudirman Kav. 29-31, Kel. Karet, Kec. Setiabudi, Jakarta Selatan, DKI Jakarta

Registration Date

Sep 13, 2022

Expiry Date

Feb 10, 2026

Product Type

Clinical Chemistry Test System

Creatinine test system (kit & cair)

Invitro Diagnostics

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