IMMULITE 1000 Substrate Module 1000T - Indonesia BPOM Medical Device Registration

IMMULITE 1000 Substrate Module 1000T is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204220151. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : A

IMMULITE 1000 Substrate Module 1000T

Analysis ID: AKL 10204220151

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

SIEMENS HEALTHCARE DIAGNOSTICS INC

Country of Origin

United States

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88

Registration Date

Feb 05, 2025

Expiry Date

Jun 25, 2029

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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Other Products from SIEMENS HEALTHCARE DIAGNOSTICS INC

Products from the same manufacturer (10 products)

IMMULITE 1000 Substrate Module 1000T - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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