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ZENIX Diluent - Indonesia BPOM Medical Device Registration

ZENIX Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208124042. The device is manufactured by RAYTO LIFE AND ANALYTICAL SCIENCES CO. LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
ZENIX Diluent
Analysis ID: AKL 20208124042

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Feb 01, 2024

Expiry Date

Jan 31, 2027

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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