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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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BPOM Registered
Risk Class Kelas Resiko : B
LEKSELL Stereotactic System
Analysis ID: AKL 21002122304

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Sweden

Authorized Representative

PT. MEDIUM FIRST

AR 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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