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Erba Mannheim XL SysPack CREA ENZ 200 - Indonesia BPOM Medical Device Registration

Erba Mannheim XL SysPack CREA ENZ 200 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101422209. The device is manufactured by ERBA LACHEMA S.R.O. from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ERBA DIAGNOSTIC 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
Erba Mannheim XL SysPack CREA ENZ 200
Analysis ID: AKL 20101422209

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Czech Republic

Authorized Representative

ERBA DIAGNOSTIC INDONESIA

AR Address

Ruko Tabespot G6-5, Jalan BSD Raya Pusat

Registration Date

Oct 29, 2024

Expiry Date

Apr 09, 2029

Product Type

Clinical Chemistry Test System

Creatinine test system (kit & cair)

Invitro Diagnostics

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