KELLYMED Syringe Pump - Indonesia BPOM Medical Device Registration
KELLYMED Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902124107. 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. PRIMA TUNAS SURYA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING KELLYMED CO.,LTDCountry of Origin
China
Authorized Representative
PT. PRIMA TUNAS SURYA MEDIKAAR Address
RUKO SENTRA ONDERDIL BLOK ED NOMOR 24
Registration Date
Jul 12, 2021
Expiry Date
Jun 02, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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