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RIZKIMED Endotracheal Tube Reinforced - Indonesia BPOM Medical Device Registration

RIZKIMED Endotracheal Tube Reinforced is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321749. The device is manufactured by NANCHANG KANGHUA HEALTH MATERIALS CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is RIZQULLAH MEDISKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
RIZKIMED Endotracheal Tube Reinforced
Analysis ID: AKL 20403321749

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

RIZQULLAH MEDISKA INDONESIA

AR Address

Perum Pabuaran Indah Blok i 6 No.2 Rt 012 Rw 017 Jalan Alpukat IV Pabuaran Cibinong

Registration Date

Nov 14, 2023

Expiry Date

Nov 13, 2026

Product Type

Therapeutic Anesthesia Equipment

Tracheal tube.

Non Electromedic Sterile

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