OMNI PMMA - Indonesia BPOM Medical Device Registration
OMNI PMMA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202915045. The device is manufactured by OMNI LENS PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. PERFECT SINGLE OPTICS.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
OMNI LENS PVT., LTD.Country of Origin
India
Authorized Representative
PT. PERFECT SINGLE OPTICSAR Address
Jl. Pintu Air Raya No. 36 KL. Pasar baru
Registration Date
Feb 08, 2023
Expiry Date
Jul 24, 2026
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
OMNI PMMA Intra Ocular Lens
OMNI HYAL 18 mg/mL
C-Thru Hydrophilic Acrylic Foldable IOL
C-THRU Hydrophilic Acrylic Foldable IOL
C-THRU Hydrophobic Acrylic Foldable IOL
OMNI AQUAFOLD Hydrophilic Acrylic Foldable IOL
OMNI INNOVA Aspheric Foldable IOL
OMNIDRAPE Eye Drape
OMNI Knife
OCULUS Versa HD Disposable LenZ
OCULUS OPTIKGERäTE GMBH.
EVA NEXUS Phaco vitrectomy system including laser with DORC connector
D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNATIONAL) B.V.
EVA NEXUS Phaco vitrectomy NCBF system including laser with DORC connector
D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNATIONAL) B.V.
Meridian MR Q SLT
MERIDIAN MEDICAL D.O.O.
MERIDIAN MR Q SLT
MERIDIAN MEDICAL D.O.O.
OCULUS MYOPIA MASTER
OCULUS OPTIKGERäTE GMBH
OCULUS Perimeter Smartfield
OCULUS OPTIKGERÄTE GMBH.
OCULUS Keratograph 5M
OCULUS OPTIKGERÄTE GMBH.
HMC-Anomaloskop (MR)
OCULUS OPTIKGERÄTE GMBH
BIOM® ready
OCULUS OPTIKGERÄTE GMBH.