LEKSELL Stereotactic System - Indonesia BPOM Medical Device Registration
LEKSELL Stereotactic System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002122304. The device is manufactured by ELEKTA INSTRUMENT AB. from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDIUM FIRST.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ELEKTA INSTRUMENT AB.Country of Origin
Sweden
Authorized Representative
PT. MEDIUM FIRSTAR Address
The Bellezza Permata Hijau GP Office Tower Lantai 27 No. 03, Jl. Letjen Soepeno No. 34, Jakarta
Registration Date
Apr 22, 2021
Expiry Date
Dec 31, 2023
Product Type
Surgical Neurology Equipment
Stereotaxic instrument.
Non Radiation Electromedics
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