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TECHNOMED Qapha TiM80 Patient Monitor - Indonesia BPOM Medical Device Registration

TECHNOMED Qapha TiM80 Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420433. The device is manufactured by EDAN INSTRUMENTS, INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIPUTRA TECHNO MED.

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BPOM Registered
Risk Class Kelas Resiko : B
TECHNOMED Qapha TiM80 Patient Monitor
Analysis ID: AKL 20502420433

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRIPUTRA TECHNO MED

AR Address

Jl. Metro Tanjung Bunga Ruko Sumba Opu Blok A/17

Registration Date

Oct 30, 2024

Expiry Date

Jun 11, 2027

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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