Alta™ Multipurpose Device - Indonesia BPOM Medical Device Registration
Alta™ Multipurpose Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21502220005. The device is manufactured by QFIX from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MURTI INDAH SENTOSA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
QFIXCountry of Origin
United States
Authorized Representative
PT. MURTI INDAH SENTOSAAR Address
WISMA MURTI JL. SULTAN ISKANDAR MUDA KAV. 29 ARTERI PONDOK INDAH
Registration Date
Feb 16, 2022
Expiry Date
Jan 16, 2025
Product Type
Therapeutic Radiology Equipment
Medical charged-particle radiation therapy system.
Non Electromedic Non Sterile
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