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Q-MED INTENSIFYING SCREEN, GREEN - Indonesia BPOM Medical Device Registration

Q-MED INTENSIFYING SCREEN, GREEN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501122065. The device is manufactured by SHANDONG DOUBLE EAGLE MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SRI INTAN PERKASA.

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BPOM Registered
Risk Class Kelas Resiko : A
Q-MED INTENSIFYING SCREEN, GREEN
Analysis ID: AKL 11501122065

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SRI INTAN PERKASA

AR Address

RUKO HARAPAN INDAH BLOK EN/7 KOMPLEK HARAPAN INDAH BEKASI BARAT, KOTA BEKASI, JAWA BARAT

Registration Date

Apr 13, 2021

Expiry Date

Apr 13, 2024

Product Type

Diagnostic Radiology Equipment

Radiographic intensifying screen.

Non Electromedic Non Sterile

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