ZEISS TRENION 3D HD - Indonesia BPOM Medical Device Registration
ZEISS TRENION 3D HD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903022872. The device is manufactured by CARL ZEISS MEDITEC AG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ELO KARSA UTAMA.
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
CARL ZEISS MEDITEC AGCountry of Origin
Germany
Authorized Representative
ELO KARSA UTAMAAR Address
Jl. Raya Kebayoran Lama No. 34-E, Grogol Selatan, Kebayoran Lama.
Registration Date
Mar 31, 2022
Expiry Date
May 01, 2025
Product Type
General Hospital Equipment and Other Individuals
Medical device data system
Non Radiation Electromedics
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