Atellica Direct Load - Indonesia BPOM Medical Device Registration
Atellica Direct Load is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102022675. 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, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
May 11, 2020
Expiry Date
Mar 04, 2025
Product Type
Clinical Laboratory Equipment
General purpose laboratory equipment labeled or promoted for a specific medical use. (Electrically operated)
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