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VYGON Emergency APO CPAP Kit - Indonesia BPOM Medical Device Registration

VYGON Emergency APO CPAP Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403318248. The device is manufactured by VYGON S.A from France, 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
VYGON Emergency APO CPAP Kit
Analysis ID: AKL 20403318248

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VYGON S.A

Country of Origin

France

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

Dec 06, 2022

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Anesthesia Equipment

Positive end expiratory pressure breathing attachment.

Non Electromedic Non Sterile

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