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ZENIX ZS-I Standard A Standard B - Indonesia BPOM Medical Device Registration

ZENIX ZS-I Standard A Standard B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101123905. The device is manufactured by GENRUI BIOTECH INC from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.

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BPOM Registered
Risk Class Kelas Resiko : C
ZENIX ZS-I Standard A Standard B
Analysis ID: AKL 20101123905

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

GENRUI BIOTECH INC

Country of Origin

China

Authorized Representative

PT. SUMIFIN CITRA ABADI

AR Address

Jl. Alam Sutera Boulevard Alam Sutera Town Center (ASTC) Blok 10D No.19, Kel. Pakulonan, Kec. Serpong Utara - Tangerang Selatan 15325

Registration Date

Jan 19, 2024

Expiry Date

Jan 18, 2027

Product Type

Clinical Chemistry Test System

Multi parameter clinical chemistry test system

Invitro Diagnostics

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