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ANKE CT Enhancement Injector ASA 200E - Indonesia BPOM Medical Device Registration

ANKE CT Enhancement Injector ASA 200E is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420492. The device is manufactured by SHENZHEN ANKE HIGH-TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAND MEDIKA GEMILANG.

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BPOM Registered
Risk Class Kelas Resiko : C
ANKE CT Enhancement Injector ASA 200E
Analysis ID: AKL 20501420492

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GRAND MEDIKA GEMILANG

AR Address

Ciputra Office Tower 3 Lantai 20 unit 07, Lingkar Luar Barat No. 101

Registration Date

Nov 13, 2024

Expiry Date

Apr 06, 2027

Product Type

Diagnostic Cardiology Equipment

Angiographic Injector and Syringe

Non Radiation Electromedics

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