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ELECTRO-MAG Negatoscope - Indonesia BPOM Medical Device Registration

ELECTRO-MAG Negatoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501917339. The device is manufactured by ELEKTRO-MAG LABORATUVAR ALETLERI SAN. VE TIC.A.S. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ALKESTRON SELF-SOURCE.

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BPOM Registered
Risk Class Kelas Resiko : A
ELECTRO-MAG Negatoscope

ELEKTRO-MAG Negatoscope

Analysis ID: AKL 11501917339

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Turkey

Authorized Representative

ALKESTRON SELF-SOURCE

AR Address

Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96

Registration Date

Nov 11, 2019

Expiry Date

Sep 16, 2024

Product Type

Diagnostic Radiology Equipment

Radiographic film illuminator.

Non Radiation Electromedics

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