OPHTEIS ORGANIC 1.8% - Indonesia BPOM Medical Device Registration
OPHTEIS ORGANIC 1.8% is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203812537. The device is manufactured by RAYNER INTRAOCULAR LENSES LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is BT. Encheval Putera Megatrading.
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.
OPHTEIS BIO 1.8%
Risk Classification
Product Class
Kelas : 3
Manufacturer
RAYNER INTRAOCULAR LENSES LIMITEDCountry of Origin
United Kingdom
Authorized Representative
BT. Encheval Putera MegatradingAR Address
JL PULO LENTUT NO. 10 KWS INDUSTRI PULO GADUNG
Registration Date
Nov 26, 2024
Expiry Date
Jun 01, 2029
Product Type
Surgical Eye Equipment
Intraocular fluid.
Non Electromedic Sterile
RAYONE Aspheric
RAYONE Trifocal
RAYONE Hydrophobic Aspheric
RAYONE Toric
SULCOFLEX TRIFOCAL
RAYONE EMV
OPHTEIS ORGANIC 1.6
SUPERFLEX Aspheric System Pack
C-FLEX System Pack
T-FLEX Aspheric
RAYONE Aspheric
RAYNER INTRAOCULAR LENSES LIMITED
OPHTEIS BIO 3.0
VSY BIYOTEKNOLOJI Ve IIac Sanayi Anonim Sirketi
OPHTEIS FR Pro
VSY BIYOTEKNOLOJI Ve IIac Sanayi Anonim Sirketi
RAYONE Hydrophobic Aspheric
RAYNER INTRAOCULAR LENSES LIMITED
RAYONE Trifocal
RAYNER INTRAOCULAR LENSES LIMITED
RENASYS-F Foam Dressing Kit with Soft Port (Harmac)
HARMAC MEDICAL PRODUCTS.
RAYONE Toric
RAYNER INTRAOCULAR LENSES LIMITED
SULCOFLEX TRIFOCAL
RAYNER INTRAOCULAR LENSES LIMITED
RAYONE EMV
RAYNER INTRAOCULAR LENSES LIMITED
ACCUJECT 1.8-1P Injector Set
MEDICEL AG.

