LMA Flexible Single Use - Indonesia BPOM Medical Device Registration

LMA Flexible Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403918170. The device is manufactured by PLAXTRON INDUSTRIAL (M) SDN., BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

LMA Flexible Single Use

Analysis ID: AKL 20403918170

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PLAXTRON INDUSTRIAL (M) SDN., BHD.

Country of Origin

Malaysia

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Nov 03, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Anesthesia Equipment

Oropharyngeal airway.

Non Electromedic Sterile

DJ Fang

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