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NUGRA Angiographic Catheter - Indonesia BPOM Medical Device Registration

NUGRA Angiographic Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420563. The device is manufactured by LEPU MEDICAL TECHNOLOGY (BEIJING) CO,. LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NUGRA KARSERA.

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BPOM Registered
Risk Class Kelas Resiko : C
NUGRA Angiographic Catheter
Analysis ID: AKL 20501420563

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Oct 18, 2024

Expiry Date

Aug 23, 2027

Product Type

Diagnostic Cardiology Equipment

Diagnostic intravascular catheter.

Non Electromedic Sterile

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