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PAXERAULTIMA360 - Indonesia BPOM Medical Device Registration

PAXERAULTIMA360 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501028319. The device is manufactured by PAXERAHEALTH CORP from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INMED TECHNOTAMA BRILLIANTLY.

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BPOM Registered
Risk Class Kelas Resiko : B
PAXERAULTIMA360
Analysis ID: AKL 21501028319

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PAXERAHEALTH CORP

Country of Origin

United States

Authorized Representative

PT. INMED TECHNOTAMA BRILLIANTLY

AR Address

Rukan Inkopau Ujung Menteng Blok B No. 31, Il. Sultan Hamengkubuwono IX Km. 25, Kel. Ujung Menteng Kec. Cakung

Registration Date

Jan 01, 2021

Expiry Date

Sep 09, 2025

Product Type

Diagnostic Radiology Equipment

(Dihapus) Picture archiving and communications system.

Non Radiation Electromedics

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