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Respons 910 Complete - Indonesia BPOM Medical Device Registration

Respons 910 Complete is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102320575. The device is manufactured by BIT ANALYTICAL INSTRUMENTS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is Sysmex 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
Respons 910 Complete
Analysis ID: AKL 10102320575

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

Sysmex Indonesia

AR Address

Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13

Registration Date

Jul 20, 2023

Expiry Date

Mar 03, 2028

Product Type

Clinical Laboratory Equipment

Colorimeter, photometer, or spectrophotometer for clinical use.

Invitro Diagnostics

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