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CANACK Laryngeal Mask Airway (LMA) - Indonesia BPOM Medical Device Registration

CANACK Laryngeal Mask Airway (LMA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403916244. The device is manufactured by NINGBO LUKE MEDICAL DEVICES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOMEDIKA SOLUSINDO.

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BPOM Registered
Risk Class Kelas Resiko : B
CANACK Laryngeal Mask Airway (LMA)
Analysis ID: AKL 20403916244

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDOMEDIKA SOLUSINDO

AR Address

GRIYA KAYU PUTIH I Jl. Kayu Mas Raya No. 1/Q Kelurahan Pulogadung Kecamatan Pulogadung

Registration Date

Aug 27, 2021

Expiry Date

Sep 09, 2024

Product Type

Therapeutic Anesthesia Equipment

Oropharyngeal airway.

Non Electromedic Sterile

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