Emit II Plus Ecstasy Assay - Indonesia BPOM Medical Device Registration
Emit II Plus Ecstasy Assay is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103320258. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC., USA from United States, and is classified as Risk Class Kelas Resiko : B. 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 : 2
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS INC., USACountry of Origin
United States
Authorized Representative
SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Jan 25, 2023
Expiry Date
Jan 28, 2025
Product Type
Clinical Toxicology Test System
Methamphetamine test system (kit & cair)
Invitro Diagnostics
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