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FLEXICARE Veoflo High Flow Nasal Cannula With Adapter - Indonesia BPOM Medical Device Registration

FLEXICARE Veoflo High Flow Nasal Cannula With Adapter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403021510. The device is manufactured by FLEXICARE MEDICAL (DONGGUAN) LIMITED from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BINABAKTI NIAGAPERKASA.

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BPOM Registered
Risk Class Kelas Resiko : A
FLEXICARE Veoflo High Flow Nasal Cannula With Adapter
Analysis ID: AKL 10403021510

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. BINABAKTI NIAGAPERKASA

AR Address

Jl. Kebon Jeruk I No. 32 Taman Sari Jakarta Barat

Registration Date

Nov 30, 2023

Expiry Date

Nov 06, 2026

Product Type

Therapeutic Anesthesia Equipment

Nasal oxygen cannula.

Non Electromedic Non Sterile

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DJ Fang

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