DELPHI Plus - Indonesia BPOM Medical Device Registration
DELPHI Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422518. The device is manufactured by CNS MEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FAJAR SELARAS PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CNS MEDICAL CO., LTD.Country of Origin
Korea
Authorized Representative
FAJAR SELARAS PARTNERSAR Address
RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29
Registration Date
Oct 25, 2024
Expiry Date
Oct 27, 2028
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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