CAVITIMI - Indonesia BPOM Medical Device Registration
CAVITIMI is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602028257. The device is manufactured by IMICRYL DIS MALZEMELERI SAN. VE T.S. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CIPTA MEDIKA SEMPURNA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IMICRYL DIS MALZEMELERI SAN. VE T.S. A.S.Country of Origin
Turkey
Authorized Representative
CIPTA MEDIKA SEMPURNAAR Address
JL. WR. SUPRATMAN KAV. 9 NO. 4 RT. 002/004 KEL. CEMPAKA PUTIH - KEC. CIPUTAT TIMUR
Registration Date
Dec 30, 2020
Expiry Date
Jul 08, 2025
Product Type
Prosthetic Dental Equipment
Dental cement.
Non Electromedic Non Sterile
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NOVA COMPO C
IMICRYL IMIBOND-F
IMICRCYL Biofactor MTA (Mineral Trioxide Aggregate)
IMICRYL NOVA COMPO HS
IMICRYL NOVA GLASS LC
IMICRYL Prosimi Root Canal Irrigation Gel
IMICRYL POLIMO Flouride Gel
IMICRYL IMIPRINT (Prophylaxis Paste)
IMICRYL Imipomza
PYRAX Paracam
PYRAX POLYMARS
IMICRYL BISOTIC
IMICRYL DIS MALZEMELERI SAN. VE TIC. A.S.
IMICRYL NOVA COMPO HS
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IMICRYL NOVA GLASS LC
IMICRYL DIS MALZEMELERI SAN. VE T.S. A.S.
IMICRYL IMIPRINT (Prophylaxis Paste)
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IMICRYL Nova Compo C Composite Set
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IMICRYL Zino-EG
IMICRYL DIS MALZEMELERI SAN. VE T.S. A.S.
IMICRYL Fissured Nova Plus+
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IMICRYL Nova Resin Cement
IMICRYL DIS MALZEMELERI SAN. VE T.S. A.S.
New IMICRYL Glass-L
IMICRYL DIS MALZEMELERI SAN. VE T.S. A.S.