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NUGRA Balloon Inflation Devices - Indonesia BPOM Medical Device Registration

NUGRA Balloon Inflation Devices is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320927. The device is manufactured by SCW MEDICATH 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 Balloon Inflation Devices
Analysis ID: AKL 20501320927

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SCW MEDICATH LTD.

Country of Origin

China

Authorized Representative

PT. NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Aug 01, 2023

Expiry Date

Jul 31, 2026

Product Type

Diagnostic Cardiology Equipment

Angiographic injector and syringe.

Non Electromedic Sterile

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