NIPRO SAFELET Cath - Indonesia BPOM Medical Device Registration
NIPRO SAFELET Cath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902602290. The device is manufactured by NIPRO CORPORATION ODATE FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NIPRO CORPORATION ODATE FACTORYCountry of Origin
Japan
Authorized Representative
PT. MAIN WHEEL BEAMAR Address
Perkantoran Duta Merlin Blok C No 58 jalan gajah mada
Registration Date
Oct 04, 2022
Expiry Date
Feb 17, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular catheter.
Non Electromedic Non Sterile
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