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BOSCH Vivalytic One - Indonesia BPOM Medical Device Registration

BOSCH Vivalytic One is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102420093. The device is manufactured by LRE MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.

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
BOSCH Vivalytic One
Analysis ID: AKL 20102420093

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

LRE MEDICAL GMBH

Country of Origin

Germany

Authorized Representative

PT. CEKINDO BUSINESS INTERNATIONAL

AR Address

CEKINDO BUSINESS INTERNATIONAL

Registration Date

Apr 23, 2024

Expiry Date

Nov 08, 2028

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

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