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ACCUMAX Pro Micropipette Fix Volume - Indonesia BPOM Medical Device Registration

ACCUMAX Pro Micropipette Fix Volume is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102910423. The device is manufactured by ACCUMAX LAB DEVICES PVT LTD. from India, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ENDO 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 : A
ACCUMAX Pro Micropipette Fix Volume
Analysis ID: AKL 10102910423

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

India

Authorized Representative

PT. ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Feb 13, 2019

Expiry Date

Dec 12, 2023

Product Type

Clinical Laboratory Equipment

Pipetting and diluting system for clinical use.

Invitro Diagnostics

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DJ Fang

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