BOSKA Infusion Pump - Indonesia BPOM Medical Device Registration
BOSKA Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902322173. The device is manufactured by BEIJING KELLYMED, CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KARUNIAJAYA ANDALAN PRIMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING KELLYMED, CO., LTDCountry of Origin
China
Authorized Representative
PT. KARUNIAJAYA ANDALAN PRIMAAR Address
RUKO JALUR SUTERA TIMUR BLOK. 6B NO. 23 ALAM SUTERA, SERPONG, TANGERANG 15144.
Registration Date
Jun 11, 2023
Expiry Date
May 18, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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