SHARP Medical Gas Regulator - Indonesia BPOM Medical Device Registration
SHARP Medical Gas Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402027964. The device is manufactured by SANKO MANUFACTURING CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ETERNAL MATESU.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SANKO MANUFACTURING CO., LTD.Country of Origin
Japan
Authorized Representative
ETERNAL MATESUAR Address
Jl. Jembatan Tiga No.11C Kel.Penjaringan Kec.Penjaringan - Jakarta Utara Telp : 021-6615716
Registration Date
May 21, 2024
Expiry Date
Sep 12, 2027
Product Type
Monitoring Anesthesia Equipment
Pressure regulator.
Non Electromedic Non Sterile
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