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CARESTREAM GBX DEVELOPER AND REPLENISHER - Indonesia BPOM Medical Device Registration

CARESTREAM GBX DEVELOPER AND REPLENISHER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501125080. The device is manufactured by CARESTREAM HEALTH, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MANDALA MITRATAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
CARESTREAM GBX DEVELOPER AND REPLENISHER
Analysis ID: AKL 21501125080

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MANDALA MITRATAMA

AR Address

Komplek Ruko Roxy Mas Blok C 2 No. 12 Jl. Hasyim Ashari 125

Registration Date

Jul 26, 2023

Expiry Date

Aug 31, 2025

Product Type

Diagnostic Radiology Equipment

Automatic radiographic film processor.

Non Electromedic Non Sterile

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