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GENOSS Inflator B40 - Indonesia BPOM Medical Device Registration

GENOSS Inflator B40 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501917581. The device is manufactured by COMRADE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ICT WORLDWIDE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
GENOSS Inflator B40
Analysis ID: AKL 20501917581

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

COMRADE CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. ICT WORLDWIDE INDONESIA

AR Address

Gedung Annex RS Jakarta Lt. 3, Jl. Jenderal Sudirman Kav. 49, Kel. Karet Semanggi, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos 12930

Registration Date

Jun 13, 2023

Expiry Date

Feb 18, 2026

Product Type

Diagnostic Cardiology Equipment

Angiographic Injector and Syringe

Non Electromedic Sterile

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