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IPAS MVA Plus® Manual Vacuum Aspiration (MVA) - Indonesia BPOM Medical Device Registration

IPAS MVA Plus® Manual Vacuum Aspiration (MVA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104122097. The device is manufactured by PACIFIC HOSPITAL SUPPLY CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DKT INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : B
IPAS MVA Plus® Manual Vacuum Aspiration (MVA)
Analysis ID: AKL 21104122097

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

DKT INTERNATIONAL

AR Address

GRAHA SUCOFINDO Lantai 12 Jl. Raya Pasar Minggu Kav. 34

Registration Date

Apr 13, 2021

Expiry Date

Sep 15, 2025

Product Type

Therapeutic Obstetric and Gynecological Equipment

Vacuum abortion system.

Non Electromedic Non Sterile

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