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INMEDFLATOR PTCA Inflation Device - Indonesia BPOM Medical Device Registration

INMEDFLATOR PTCA Inflation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501714410. The device is manufactured by UMBRA MEDICAL PRODUCTS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
INMEDFLATOR PTCA Inflation Device
Analysis ID: AKL 20501714410

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Apr 16, 2021

Expiry Date

Jan 01, 2024

Product Type

Diagnostic Cardiology Equipment

Angiographic injector and syringe.

Non Electromedic Sterile

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