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EDAN HD600 Diluent - Indonesia BPOM Medical Device Registration

EDAN HD600 Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208520012. The device is manufactured by EDAN INSTRUMENT, INC., from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NUSANTARA MEDCARE INDONESIA.

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
EDAN HD600 Diluent
Analysis ID: AKL 20208520012

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. NUSANTARA MEDCARE INDONESIA

AR Address

NUSANTARA MEDCARE INDONESIA

Registration Date

Jan 10, 2025

Expiry Date

Jul 31, 2027

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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