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Z-MED II ™ Percutaneous Transluminal Valvulopasty Catheter - Indonesia BPOM Medical Device Registration

Z-MED II ™ Percutaneous Transluminal Valvulopasty Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320677. The device is manufactured by NUMED INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is NUGRA KARSERA.

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BPOM Registered
Risk Class Kelas Resiko : C
Z-MED II ™ Percutaneous Transluminal Valvulopasty Catheter
Analysis ID: AKL 20501320677

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

NUMED INC.

Country of Origin

United States

Authorized Representative

NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Nov 09, 2024

Expiry Date

Dec 31, 2028

Product Type

Diagnostic Cardiology Equipment

Balloon aortic valvuloplasty catheter.

Non Electromedic Sterile

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