KERR K-FILES - Indonesia BPOM Medical Device Registration
KERR K-FILES is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603420319. The device is manufactured by ORMEX S. DE R.L. DE C.V., from Mexico, 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
ORMEX S. DE R.L. DE C.V.,Country of Origin
Mexico
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
Sep 03, 2024
Expiry Date
Jan 26, 2027
Product Type
Surgical Dental Equipment
Dental hand instrument
Non Electromedic Non Sterile
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