STERIS V-PRO MAX 2 Double Door Low Temperature Sterilization System - Indonesia BPOM Medical Device Registration
STERIS V-PRO MAX 2 Double Door Low Temperature Sterilization System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903020267. The device is manufactured by STERIS MEXICO. S. DE R.L DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
STERIS MEXICO. S. DE R.L DE C.V.Country of Origin
Mexico
Authorized Representative
PT. INDOMEDIK NIAGA PERKASAAR Address
JALAN RAYA KEBAYORAN LAMA NO.35 RT.008 RW.001 Kel. Sukabumi Selatan Kec, Kebon Jeruk, Jakarta Barat, provinsi DKI Jakarta
Registration Date
Oct 27, 2023
Expiry Date
Aug 19, 2026
Product Type
General Hospital Equipment and Other Individuals
Steam sterilizer.
Non Radiation Electromedics
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