LEFORTE System Bone Plate - Indonesia BPOM Medical Device Registration
LEFORTE System Bone Plate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603916111. The device is manufactured by JEIL MEDICAL CORPORATION 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
JEIL MEDICAL CORPORATIONCountry of Origin
Korea
Authorized Representative
FAJAR SELARAS PARTNERSAR Address
RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29
Registration Date
Aug 04, 2024
Expiry Date
Jul 04, 2029
Product Type
Surgical Dental Equipment
Bone plate.
Non Electromedic Non Sterile
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