KERR OptiDam Frame - Indonesia BPOM Medical Device Registration
KERR OptiDam Frame is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605520017. The device is manufactured by KERR ITALIA, S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TIGASATU MEDIKA SOLUSINDO.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 1
Manufacturer
KERR ITALIA, S.R.L.Country of Origin
Italy
Authorized Representative
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
Jan 04, 2025
Expiry Date
Jan 26, 2027
Product Type
Other Dental Equipment
Rubber dam and accessories.
Non Electromedic Non Sterile
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