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RAYTO DILUENT - Indonesia BPOM Medical Device Registration

RAYTO DILUENT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208121065. 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. WHIRA PITOE USAHABERSAMA.

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
RAYTO DILUENT
Analysis ID: AKL 20208121065

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. WHIRA PITOE USAHABERSAMA

AR Address

RUKO BUARAN PERSADA NO. 10, JL. JEND.POL.SOEKAMTO RT.008/06,KEL.DUREN SAWIT

Registration Date

Jun 10, 2024

Expiry Date

Jan 18, 2029

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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