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FLEXICARE Adult Single Heated Wire Breathing System 22mm 1.6m Water Trap and Auto Fill Chamber - Indonesia BPOM Medical Device Registration

FLEXICARE Adult Single Heated Wire Breathing System 22mm 1.6m Water Trap and Auto Fill Chamber is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403026085. 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 BINABAKTI NIAGAPERKASA.

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BPOM Registered
Risk Class Kelas Resiko : A
FLEXICARE Adult Single Heated Wire Breathing System 22mm 1.6m Water Trap and Auto Fill Chamber
Analysis ID: AKL 10403026085

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

BINABAKTI NIAGAPERKASA

AR Address

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

Registration Date

Jul 29, 2022

Expiry Date

Jan 21, 2025

Product Type

Therapeutic Anesthesia Equipment

Anesthesia breathing circuit.

Non Electromedic Sterile

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