KERR SEALAPEX - Indonesia BPOM Medical Device Registration
KERR SEALAPEX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420359. The device is manufactured by KERR CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TIGASATU MEDIKA SOLUSINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KERR CORPORATIONCountry of Origin
United States
Authorized Representative
PT. TIGASATU MEDIKA SOLUSINDOAR Address
Karawaci Office Park, Jalan Imam Bonjol, Ruko Finangsia Blok H 53, Prov. Banten, Kota Tangerang, Kec. Cibodas, Kel. Panunggangan Barat
Registration Date
Sep 12, 2024
Expiry Date
Jan 26, 2027
Product Type
Prosthetic Dental Equipment
Root canal filling resin
Non Electromedic Non Sterile
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