OASIS Inpatient Room Instrument Set - Indonesia BPOM Medical Device Registration
OASIS Inpatient Room Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603026911. The device is manufactured by OASIS TECHNOLOGY PTE. LTD. from Hong Kong (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MULTI SCIENCE PATSAIC.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
OASIS TECHNOLOGY PTE. LTD.Country of Origin
Hong Kong (China)
Authorized Representative
MULTI SCIENCE PATSAICAR Address
JL. SUKAMULYA NO. 61
Registration Date
Jun 13, 2024
Expiry Date
Mar 05, 2027
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile

