CHEST HI-301 Spirometry System - Indonesia BPOM Medical Device Registration
CHEST HI-301 Spirometry System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401815653. The device is manufactured by CHEST MIYAGI FACTORY. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CHEST MIYAGI FACTORY.Country of Origin
Japan
Authorized Representative
PT. IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Sep 02, 2023
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Anesthesia Equipment
Diagnostic spirometer.
Non Radiation Electromedics
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