ADVIA 120/ADVIA 2120/ADVIA 2120i EZ WASH. - Indonesia BPOM Medical Device Registration
ADVIA 120/ADVIA 2120/ADVIA 2120i EZ WASH. is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204126750. 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.
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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS INC.Country of Origin
United States
Authorized Representative
SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Jan 09, 2025
Expiry Date
Aug 01, 2029
Product Type
Reagents and Specimen Providers
General purpose reagent.
Invitro Diagnostics
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