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ResAppDx - Indonesia BPOM Medical Device Registration

ResAppDx is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401125321. The device is manufactured by RESAPP HEALTH LTD from Australia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ASIA ACTUAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
ResAppDx
Analysis ID: AKL 20401125321

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

RESAPP HEALTH LTD

Country of Origin

Australia

Authorized Representative

PT. ASIA ACTUAL INDONESIA

AR Address

PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN

Registration Date

Aug 30, 2021

Expiry Date

Jun 21, 2026

Product Type

Diagnostic Anesthesia Equipment

Predictive pulmonary-function value calculator.

Non Electromedic Non Sterile

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