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ANARA MEDICAL Endotracheal Tube - Indonesia BPOM Medical Device Registration

ANARA MEDICAL Endotracheal Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420750. The device is manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANARA TRISAKTI MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
ANARA MEDICAL Endotracheal Tube
Analysis ID: AKL 20403420750

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ANARA TRISAKTI MEDIKA

AR Address

Jl. Pondok Kelapa Raya. Komplek Ruko Taman Pondok Kelapa Blok A no 6-7, Prov. DKI Jakarta, Kota Jakarta Timur, Kec. Duren Sawit, Kel. Pondok Kelapa

Registration Date

Nov 09, 2024

Expiry Date

Nov 06, 2027

Product Type

Therapeutic Anesthesia Equipment

Tracheal tube.

Non Electromedic Sterile

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