Chek-Stix Liquid QC Kit + Sediment - Indonesia BPOM Medical Device Registration

Chek-Stix Liquid QC Kit + Sediment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322731. The device is manufactured by KOVA INTERNATIONAL, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

Chek-Stix Liquid QC Kit + Sediment

Analysis ID: AKL 20101322731

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

KOVA INTERNATIONAL, INC.

Country of Origin

United States

Authorized Representative

PT. SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta

Registration Date

Mar 07, 2023

Expiry Date

Apr 22, 2027

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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